A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153702



Internal ID15874229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44941778..45041042hg38UCSC Ensembl
Innerchr6:44909515..45008779hg19UCSC Ensembl
Innerchr6:45017493..45116757hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3899265
hg1999265
hg1899265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603007
Supporting Variants
SamplesHGDP00491
Known GenesSUPT3H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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