A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075172



Internal ID15928358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160611057..160646860hg38UCSC Ensembl
Innerchr6:161032089..161067892hg19UCSC Ensembl
Innerchr6:160952079..160987882hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3835804
hg1935804
hg1835804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605000
Supporting Variants
Samples
Known GenesLPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075172
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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