A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440798



Internal ID21098351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84167671..84172371hg38UCSC Ensembl
chr10:85927427..85932127hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384701
hg194701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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