A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674193



Internal ID18972474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146321181..146337763hg38UCSC Ensembl
Innerchr7:146018273..146034855hg19UCSC Ensembl
Innerchr7:145649206..145665788hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3816583
hg1916583
hg1816583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022058
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)nssv3674193
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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