A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604475



Internal ID16045198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108291332..108295119hg38UCSC Ensembl
Innerchr6:108612536..108616323hg19UCSC Ensembl
Innerchr6:108719229..108723016hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383788
hg193788
hg183788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071951
Samples
Known GenesLACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604475
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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