A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697169



Internal ID15087135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76962203..77035230hg38UCSC Ensembl
Innerchr15:77254544..77327571hg19UCSC Ensembl
Innerchr15:75041599..75114626hg18UCSC Ensembl
Innerchr15:75041599..75114626hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3873028
hg1973028
hg1873028
hg1773028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517068
Supporting Variants
Samples
Known GenesPSTPIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697169
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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