A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604790



Internal ID16392199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141808872..141915441hg38UCSC Ensembl
Innerchr6:142130009..142236578hg19UCSC Ensembl
Innerchr6:142171702..142278271hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38106570
hg19106570
hg18106570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155786
SamplesHGDP01251
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604790
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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