A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1071829



Internal ID15578329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104813138..104814218hg38UCSC Ensembl
Innerchr6:105261013..105262093hg19UCSC Ensembl
Innerchr6:105367706..105368786hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381081
hg191081
hg181081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604416
Supporting Variants
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1071829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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