A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324942



Internal ID20858072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110883718..110884299hg38UCSC Ensembl
chr1:111426340..111426921hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050880
Samples
Known GenesCD53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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