A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701937



Internal ID15091903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76340146..76369584hg38UCSC Ensembl
Innerchr15:76632487..76661925hg19UCSC Ensembl
Innerchr15:74419542..74448980hg18UCSC Ensembl
Innerchr15:74419542..74448980hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3829439
hg1929439
hg1829439
hg1729439
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525769
Supporting Variants
Samples
Known GenesISL2, SCAPER
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701937
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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