A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642960



Internal ID18594555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12125367..12212164hg38UCSC Ensembl
Innerchr7:12164993..12251790hg19UCSC Ensembl
Innerchr7:12131518..12218315hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3886798
hg1986798
hg1886798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021710
Supporting Variants
Samples
Known GenesTMEM106B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642960
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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