A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434642



Internal ID21092195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100526532..100527102hg38UCSC Ensembl
chr8:101538760..101539330hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161354
Samples
Known GenesANKRD46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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