A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691473



Internal ID15428125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24359755..24405877hg38UCSC Ensembl
Innerchr15:24604902..24651024hg19UCSC Ensembl
Innerchr15:22155995..22202117hg18UCSC Ensembl
Innerchr15:22155995..22202117hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3846123
hg1946123
hg1846123
hg1746123
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691473
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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