A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516903



Internal ID15444196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73256383..73263193hg38UCSC Ensembl
Innerchr8:74168618..74175428hg19UCSC Ensembl
Innerchr8:74331172..74337982hg18UCSC Ensembl
Innerchr8:74331172..74337982hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg386811
hg196811
hg186811
hg176811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654794, nssv680786, nssv676191, nssv679687
Samples
Known GenesLOC100130301
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516903
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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