A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604149



Internal ID16391558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92802607..92860714hg38UCSC Ensembl
Innerchr6:93512325..93570432hg19UCSC Ensembl
Innerchr6:93569046..93627153hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3858108
hg1958108
hg1858108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155765, nssv1068410
SamplesHGDP01336
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604149
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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