A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075177



Internal ID15928363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160611449..160647288hg38UCSC Ensembl
Innerchr6:161032481..161068320hg19UCSC Ensembl
Innerchr6:160952471..160988310hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3835840
hg1935840
hg1835840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605003
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)nssv1075177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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