A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604646



Internal ID16392055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:128100617..128210506hg38UCSC Ensembl
Innerchr6:128421762..128531651hg19UCSC Ensembl
Innerchr6:128463455..128573344hg18UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38109890
hg19109890
hg18109890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10930n54
Supporting Variantsnssv1072618
Samples
Known GenesPTPRK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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