A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074141



Internal ID15927327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143548325..143550667hg38UCSC Ensembl
Innerchr6:143869462..143871804hg19UCSC Ensembl
Innerchr6:143911155..143913497hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382343
hg192343
hg182343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604799
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)nssv1074141
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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