A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604797



Internal ID16392206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143548325..143550439hg38UCSC Ensembl
Innerchr6:143869462..143871576hg19UCSC Ensembl
Innerchr6:143911155..143913269hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382115
hg192115
hg182115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10956n54
Supporting Variantsnssv1074139, nssv1074138
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604797
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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