A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515708



Internal ID15443319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136651246..136851516hg38UCSC Ensembl
Innerchr8:137663489..137863759hg19UCSC Ensembl
Innerchr8:137732671..137932941hg18UCSC Ensembl
Innerchr8:137732671..137932941hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38200271
hg19200271
hg18200271
hg17200271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693320, nssv691740, nssv658312, nssv687993, nssv704893, nssv684215, nssv684000, nssv677181, nssv682214, nssv654716, nssv665846, nssv657730, nssv667609, nssv670145, nssv677563, nssv674812, nssv665508, nssv662613, nssv684308, nssv667041, nssv691342, nssv683731, nssv670869, nssv691562, nssv679934, nssv673626, nssv666933, nssv683937, nssv686058, nssv670132, nssv690855, nssv672462, nssv662336, nssv673521, nssv654555, nssv689807, nssv667481, nssv689160, nssv669416, nssv679553, nssv672558, nssv659952, nssv689560, nssv678497, nssv655437, nssv683353, nssv660043, nssv688350, nssv665600, nssv659044, nssv691576, nssv652009, nssv678261, nssv663365, nssv656315, nssv666771, nssv668147, nssv659062, nssv664420, nssv663746, nssv654088, nssv674861, nssv658568, nssv695269, nssv676094, nssv656033, nssv654975, nssv658957, nssv687786, nssv679310, nssv667698, nssv688876, nssv655926, nssv655197, nssv657854, nssv669459, nssv667872, nssv660221, nssv688605, nssv685547, nssv669289, nssv687568, nssv666140, nssv674397, nssv687375, nssv682040, nssv673835
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515708
Frequency
Sample Size2026
Observed Gain0
Observed Loss87
Observed Complex0
Frequencyn/a


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