A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603390



Internal ID16390799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64261543..64308792hg38UCSC Ensembl
Innerchr6:64971436..65018685hg19UCSC Ensembl
Innerchr6:65029395..65076644hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3847250
hg1947250
hg1847250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1061735, nssv1154316
SamplesNINDS_222
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603390
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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