A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705725



Internal ID15442377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15677772..15892234hg38UCSC Ensembl
Innerchr3:15719279..15933741hg19UCSC Ensembl
Innerchr3:15694283..15908745hg18UCSC Ensembl
Innerchr3:15694283..15908745hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38214463
hg19214463
hg18214463
hg17214463
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529014
Supporting Variants
Samples
Known GenesANKRD28, MIR563
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705725
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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