A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1098078



Internal ID15951264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:147582855..147585235hg38UCSC Ensembl
Innerchr7:147279947..147282327hg19UCSC Ensembl
Innerchr7:146910880..146913260hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg382381
hg192381
hg182381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608958
Supporting Variants
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1098078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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