A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600735



Internal ID16388144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165391..233750hg38UCSC Ensembl
Innerchr6:165391..233750hg19UCSC Ensembl
Innerchr6:110391..178750hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3868360
hg1968360
hg1868360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10256n54
Supporting Variantsnssv1047553
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600735
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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