A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155775



Internal ID15872643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93210932..93233399hg38UCSC Ensembl
Innerchr6:93920650..93943117hg19UCSC Ensembl
Innerchr6:93977371..93999838hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3822468
hg1922468
hg1822468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604161
Supporting Variants
SamplesHGDP00005
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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