A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074133



Internal ID15927319
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 StatusS
Merged Variantsnsv604789
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)nssv1074133
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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