A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435741



Internal ID21093294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62175575..62183418hg38UCSC Ensembl
chr10:63935334..63943177hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg387844
hg197844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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