A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436340



Internal ID21093893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55443298..55787286hg38UCSC Ensembl
chr10:57203058..57547046hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38343989
hg19343989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982014
Samples
Known GenesMTRNR2L5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436340
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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