A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441882



Internal ID21099435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119623744..119624511hg38UCSC Ensembl
chr10:121383256..121384023hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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