A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605079



Internal ID16045802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162143022..162288916hg38UCSC Ensembl
Innerchr6:162564054..162709948hg19UCSC Ensembl
Innerchr6:162484044..162629938hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38145895
hg19145895
hg18145895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11004n54
Supporting Variantsnssv1075385
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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