A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435142



Internal ID21092695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33097398..33097780hg38UCSC Ensembl
chr8:32954916..32955298hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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