A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604789



Internal ID16392198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141752887..141791318hg38UCSC Ensembl
Innerchr6:142074024..142112455hg19UCSC Ensembl
Innerchr6:142115717..142154148hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3838432
hg1938432
hg1838432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074133
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604789
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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