A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674218



Internal ID18972499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146647013..146744970hg38UCSC Ensembl
Innerchr7:146344105..146442062hg19UCSC Ensembl
Innerchr7:145975038..146072995hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3897958
hg1997958
hg1897958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021923
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)nssv3674218
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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