A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705664



Internal ID15442316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56196961..56212400hg38UCSC Ensembl
Innerchr15:56489159..56504598hg19UCSC Ensembl
Innerchr15:54276451..54291890hg18UCSC Ensembl
Innerchr15:54276451..54291890hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3815440
hg1915440
hg1815440
hg1715440
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528965
Supporting Variants
Samples
Known GenesRFX7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705664
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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