A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674217



Internal ID18972498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146629723..146670701hg38UCSC Ensembl
Innerchr7:146326815..146367793hg19UCSC Ensembl
Innerchr7:145957748..145998726hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3840979
hg1940979
hg1840979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034346
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)nssv3674217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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