A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608965



Internal ID16049688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:147815527..147886588hg38UCSC Ensembl
Innerchr7:147512619..147583680hg19UCSC Ensembl
Innerchr7:147143552..147214613hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3871062
hg1971062
hg1871062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155923
SamplesHGDP00822
Known GenesCNTNAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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