A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697845



Internal ID15434497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85751825..85753010hg38UCSC Ensembl
Innerchr15:86295056..86296241hg19UCSC Ensembl
Innerchr15:84096060..84097245hg18UCSC Ensembl
Innerchr15:84096060..84097245hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381186
hg191186
hg181186
hg171186
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516322
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697845
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