A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1100633



Internal ID15953819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158051695..158122459hg38UCSC Ensembl
Innerchr7:157844387..157915151hg19UCSC Ensembl
Innerchr7:157537148..157607912hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3870765
hg1970765
hg1870765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609260
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)nssv1100633
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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