A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609356



Internal ID16396765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158311152..158437903hg38UCSC Ensembl
Innerchr7:158103844..158230595hg19UCSC Ensembl
Innerchr7:157796605..157923356hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38126752
hg19126752
hg18126752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1101687
Samples
Known GenesPTPRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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