A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604486



Internal ID16391895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:109910848..109969475hg38UCSC Ensembl
Innerchr6:110232051..110290678hg19UCSC Ensembl
Innerchr6:110338744..110397371hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3858628
hg1958628
hg1858628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071963
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604486
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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