A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020765



Internal ID19109983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11482492..11534129hg38UCSC Ensembl
Innerchr7:11522119..11573756hg19UCSC Ensembl
Innerchr7:11488644..11540281hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3851638
hg1951638
hg1851638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642934
Samples
Known GenesTHSD7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020765
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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