A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755311



Internal ID18706906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:71750208..71802242hg38UCSC Ensembl
Innerchr7:71215193..71267227hg19UCSC Ensembl
Innerchr7:70853129..70905163hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3852035
hg1952035
hg1852035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033922
Supporting Variants
Samples
Known GenesCALN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755311
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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