A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074143



Internal ID15927329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143548325..143551173hg38UCSC Ensembl
Innerchr6:143869462..143872310hg19UCSC Ensembl
Innerchr6:143911155..143914003hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382849
hg192849
hg182849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604800
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074143
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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