A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604438



Internal ID16045161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:105256293..105421255hg38UCSC Ensembl
Innerchr6:105704168..105869130hg19UCSC Ensembl
Innerchr6:105810861..105975823hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38164963
hg19164963
hg18164963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071887
Samples
Known GenesPREP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604438
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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