A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609260



Internal ID16396669
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 StatusM
Merged Variants
Supporting Variantsnssv1100633
Samples
Known GenesPTPRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609260
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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