A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523372



Internal ID15450665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163436764..163452530hg38UCSC Ensembl
Innerchr1:163406554..163422320hg19UCSC Ensembl
Innerchr1:161673178..161688944hg18UCSC Ensembl
Innerchr1:160138212..160153978hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3815767
hg1915767
hg1815767
hg1715767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699121
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523372
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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