A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701976



Internal ID15091942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30644082..31032328hg38UCSC Ensembl
Innerchr15:30936285..31324531hg19UCSC Ensembl
Innerchr15:28723577..29111823hg18UCSC Ensembl
Innerchr15:28723577..29111823hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38388247
hg19388247
hg18388247
hg17388247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525795
Supporting Variants
Samples
Known GenesFAN1, HERC2P10, LOC100288637, MIR7976, MTMR10, TRPM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701976
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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