A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603001



Internal ID16390410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:43988878..44039709hg38UCSC Ensembl
Innerchr6:43956615..44007446hg19UCSC Ensembl
Innerchr6:44064593..44115424hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3850832
hg1950832
hg1850832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153699
SamplesNINDS_55
Known GenesC6orf223
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603001
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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