A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517561



Internal ID15444854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85172982..85282336hg38UCSC Ensembl
Innerchr15:85716213..85825567hg19UCSC Ensembl
Innerchr15:83517217..83626571hg18UCSC Ensembl
Innerchr15:83517217..83626571hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38109355
hg19109355
hg18109355
hg17109355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672894, nssv656004, nssv668630, nssv692146, nssv676502, nssv660930
Samples
Known GenesLOC440300, LOC642423
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517561
Frequency
Sample Size2026
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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