A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600976



Internal ID16388385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9537378..9583119hg38UCSC Ensembl
Innerchr6:9537611..9583352hg19UCSC Ensembl
Innerchr6:9645597..9691338hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3845742
hg1945742
hg1845742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153626
Samples1780846029_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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