A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608932



Internal ID16049655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146492560..146547115hg38UCSC Ensembl
Innerchr7:146189652..146244207hg19UCSC Ensembl
Innerchr7:145820585..145875140hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3854556
hg1954556
hg1854556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1097940
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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