A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075178



Internal ID15928364
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 StatusS
Merged Variantsnsv605004
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)nssv1075178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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