A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608928



Internal ID16049651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146231337..146255854hg38UCSC Ensembl
Innerchr7:145928429..145952946hg19UCSC Ensembl
Innerchr7:145559362..145583879hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3824518
hg1924518
hg1824518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1097936
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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