A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602840



Internal ID16043563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33755606..33801120hg38UCSC Ensembl
Innerchr6:33723383..33768897hg19UCSC Ensembl
Innerchr6:33831361..33876875hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3845515
hg1945515
hg1845515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10610n54
Supporting Variantsnssv1057784
Samples
Known GenesLEMD2, MLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602840
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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