A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436404



Internal ID21093957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120353625..120359135hg38UCSC Ensembl
chr10:122113137..122118647hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg385511
hg195511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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