A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642968



Internal ID18594563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12469601..12513591hg38UCSC Ensembl
Innerchr7:12509227..12553217hg19UCSC Ensembl
Innerchr7:12475752..12519742hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3843991
hg1943991
hg1843991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017055
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642968
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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