A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154022



Internal ID15880054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255474..4472353hg38UCSC Ensembl
Innerchr6:4255708..4472587hg19UCSC Ensembl
Innerchr6:4200707..4417586hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38216880
hg19216880
hg18216880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600865
Supporting Variants
SamplesNINDS_147
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154022
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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