A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605554



Internal ID16046277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170263653..170308522hg38UCSC Ensembl
Innerchr6:170572741..170617610hg19UCSC Ensembl
Innerchr6:170414666..170459535hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3844870
hg1944870
hg1844870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155825
Samples1780862019_A
Known GenesDLL1, FAM120B, FLJ38122
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605554
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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