A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674212



Internal ID18972493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146529206..146570165hg38UCSC Ensembl
Innerchr7:146226298..146267257hg19UCSC Ensembl
Innerchr7:145857231..145898190hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3840960
hg1940960
hg1840960
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028223
Supporting Variants
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674212
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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