A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677654



Internal ID15067620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89803630..89806327hg38UCSC Ensembl
Innerchr15:90346861..90349558hg19UCSC Ensembl
Innerchr15:88147865..88150562hg18UCSC Ensembl
Innerchr15:88147865..88150562hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382698
hg192698
hg182698
hg172698
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519689
Supporting Variants
Samples
Known GenesANPEP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677654
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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