A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600805



Internal ID16388214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:829223..877878hg38UCSC Ensembl
Innerchr6:829223..877878hg19UCSC Ensembl
Innerchr6:774223..822878hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3848656
hg1948656
hg1848656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1048586
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600805
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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