A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605002



Internal ID16392411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160611449..160646870hg38UCSC Ensembl
Innerchr6:161032481..161067902hg19UCSC Ensembl
Innerchr6:160952471..160987892hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3835422
hg1935422
hg1835422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10988n54
Supporting Variantsnssv1075176, nssv1075175
Samples
Known GenesLPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605002
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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