A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446889



Internal ID21104442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75242987..75351348hg38UCSC Ensembl
chr10:77002745..77111106hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38108362
hg19108362
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178252
Samples
Known GenesZNF503-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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