A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525004



Internal ID15452297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131943942..131947549hg38UCSC Ensembl
Innerchr7:131628701..131632308hg19UCSC Ensembl
Innerchr7:131279241..131282848hg18UCSC Ensembl
Innerchr7:131085956..131089563hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg383608
hg193608
hg183608
hg173608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701038
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525004
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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