A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600866



Internal ID16388275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255474..4481187hg38UCSC Ensembl
Innerchr6:4255708..4481421hg19UCSC Ensembl
Innerchr6:4200707..4426420hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38225714
hg19225714
hg18225714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10278n54
Supporting Variantsnssv1154023
SamplesNINDS_271
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600866
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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