A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153383



Internal ID15533389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165391..274847hg38UCSC Ensembl
Innerchr6:165391..274847hg19UCSC Ensembl
Innerchr6:110391..219847hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38109457
hg19109457
hg18109457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600736
Supporting Variants
SamplesNINDS_15
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153383
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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