A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524639



Internal ID15451932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183817975..183819971hg38UCSC Ensembl
Innerchr3:183535763..183537759hg19UCSC Ensembl
Innerchr3:185018457..185020453hg18UCSC Ensembl
Innerchr3:185018465..185020461hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381997
hg191997
hg181997
hg171997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700604
Samples
Known GenesMAP6D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524639
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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