A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661383



Internal ID15051349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77017078..77088880hg38UCSC Ensembl
Innerchr15:77309419..77381222hg19UCSC Ensembl
Innerchr15:75096474..75168277hg18UCSC Ensembl
Innerchr15:75096474..75168277hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3871803
hg1971804
hg1871804
hg1771804
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517068
Supporting Variants
Samples
Known GenesPSTPIP1, TSPAN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661383
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer