A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601089



Internal ID16041812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19837856..19839050hg38UCSC Ensembl
Innerchr6:19838087..19839281hg19UCSC Ensembl
Innerchr6:19946066..19947260hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381195
hg191195
hg181195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1050876
Samples
Known GenesID4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601089
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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