A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604643



Internal ID16045366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:128038217..128172846hg38UCSC Ensembl
Innerchr6:128359362..128493991hg19UCSC Ensembl
Innerchr6:128401055..128535684hg18UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38134630
hg19134630
hg18134630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072615
Samples
Known GenesPTPRK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604643
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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