A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359693



Internal ID21017246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34437231..34494618hg38UCSC Ensembl
chr3:34478723..34536110hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3857388
hg1957388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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