A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072614



Internal ID15579114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:127957653..128029998hg38UCSC Ensembl
Innerchr6:128278798..128351143hg19UCSC Ensembl
Innerchr6:128320491..128392836hg18UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3872346
hg1972346
hg1872346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604642
Supporting Variants
Samples
Known GenesPTPRK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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