A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605008



Internal ID16392417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160832453..160849587hg38UCSC Ensembl
Innerchr6:161253485..161270619hg19UCSC Ensembl
Innerchr6:161173475..161190609hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3817135
hg1917135
hg1817135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10990n54
Supporting Variantsnssv1075182
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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