A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604435



Internal ID16391844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104940684..104941599hg38UCSC Ensembl
Innerchr6:105388559..105389474hg19UCSC Ensembl
Innerchr6:105495252..105496167hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38916
hg19916
hg18916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10895n54
Supporting Variantsnssv1071879, nssv1071880
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604435
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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