A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604843



Internal ID16392252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148531189..148570588hg38UCSC Ensembl
Innerchr6:148852325..148891724hg19UCSC Ensembl
Innerchr6:148894018..148933417hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3839400
hg1939400
hg1839400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074348
Samples
Known GenesSASH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604843
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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