A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362755



Internal ID21020308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46026101..46027400hg38UCSC Ensembl
chr3:46067593..46068892hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100678
Samples
Known GenesXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362755
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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