A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373602



Internal ID21031155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70513917..70514600hg38UCSC Ensembl
chr3:70563068..70563751hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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