A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601122



Internal ID16388531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22928604..23067445hg38UCSC Ensembl
Innerchr6:22928833..23067673hg19UCSC Ensembl
Innerchr6:23036812..23175652hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38138842
hg19138841
hg18138841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10325n54
Supporting Variantsnssv1051100
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601122
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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