A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362946



Internal ID21020499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21445545..21476381hg38UCSC Ensembl
chr3:21487037..21517873hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3830837
hg1930837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098619
Samples
Known GenesZNF385D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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