A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438188



Internal ID21095741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50869901..50871100hg38UCSC Ensembl
chr10:52629661..52630860hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981514
Samples
Known GenesA1CF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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