A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755462



Internal ID19053743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101484174hg38UCSC Ensembl
Innerchr7:100968363..101127455hg19UCSC Ensembl
Innerchr7:100755083..100914175hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38159093
hg19159093
hg18159093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024733
Supporting Variants
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755462
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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