A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1100632



Internal ID15953818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157941622..158170195hg38UCSC Ensembl
Innerchr7:157734314..157962887hg19UCSC Ensembl
Innerchr7:157427075..157655648hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38228574
hg19228574
hg18228574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609259
Supporting Variants
Samples
Known GenesPTPRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1100632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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