A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1098079



Internal ID15951265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:147582908..147585926hg38UCSC Ensembl
Innerchr7:147280000..147283018hg19UCSC Ensembl
Innerchr7:146910933..146913951hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg383019
hg193019
hg183019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608959
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)nssv1098079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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