A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705117



Internal ID15095083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64756110..64763844hg38UCSC Ensembl
Innerchr15:65048309..65056043hg19UCSC Ensembl
Innerchr15:62835362..62843096hg18UCSC Ensembl
Innerchr15:62835362..62843096hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg387735
hg197735
hg187735
hg177735
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528510
Supporting Variants
Samples
Known GenesMIR1272, RBPMS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705117
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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