A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363083



Internal ID21020636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33895601..33896600hg38UCSC Ensembl
chr3:33937093..33938092hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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