A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053558



Internal ID15560058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31903977..31907478hg38UCSC Ensembl
Innerchr6:31871754..31875255hg19UCSC Ensembl
Innerchr6:31979733..31983234hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383502
hg193502
hg183502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601965
Supporting Variants
Samples
Known GenesC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053558
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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