A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600830



Internal ID16388239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2578743..2604492hg38UCSC Ensembl
Innerchr6:2578977..2604726hg19UCSC Ensembl
Innerchr6:2523976..2549725hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3825750
hg1925750
hg1825750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154020
Samples1780854444_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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