A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686809



Internal ID15423461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94509140..94533908hg38UCSC Ensembl
Innerchr15:95052369..95077137hg19UCSC Ensembl
Innerchr15:92853373..92878141hg18UCSC Ensembl
Innerchr15:92853373..92878141hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3824769
hg1924769
hg1824769
hg1724769
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520465
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686809
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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