A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605004



Internal ID16392413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160611793..160647144hg38UCSC Ensembl
Innerchr6:161032825..161068176hg19UCSC Ensembl
Innerchr6:160952815..160988166hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3835352
hg1935352
hg1835352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10988n54
Supporting Variantsnssv1075178
Samples
Known GenesLPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605004
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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