A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526636



Internal ID15453929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:30695176..30701621hg38UCSC Ensembl
Innerchr4:30696798..30703243hg19UCSC Ensembl
Innerchr4:30305896..30312341hg18UCSC Ensembl
Innerchr4:30373067..30379512hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg386446
hg196446
hg186446
hg176446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702958
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526636
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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