A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523568



Internal ID15450861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13665574..13678128hg38UCSC Ensembl
Innerchr1:13992069..14004623hg19UCSC Ensembl
Innerchr1:13864656..13877210hg18UCSC Ensembl
Innerchr1:13737375..13749929hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3812555
hg1912555
hg1812555
hg1712555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699350
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523568
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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