A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438744



Internal ID21096297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102183568..102215318hg38UCSC Ensembl
chr10:103943325..103975075hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3831751
hg1931751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438744
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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