A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527629



Internal ID15454922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37656262..37661482hg38UCSC Ensembl
Innerchr1:38121934..38127154hg19UCSC Ensembl
Innerchr1:37894521..37899741hg18UCSC Ensembl
Innerchr1:37791027..37796247hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385221
hg195221
hg185221
hg175221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704097
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527629
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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