A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697106



Internal ID15087072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29128178..29128851hg38UCSC Ensembl
Innerchr15:29420381..29421054hg19UCSC Ensembl
Innerchr15:27207673..27208346hg18UCSC Ensembl
Innerchr15:27207673..27208346hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38674
hg19674
hg18674
hg17674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515798
Supporting Variants
Samples
Known GenesFAM189A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697106
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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