A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372079



Internal ID21029632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7810175..7950063hg38UCSC Ensembl
chr3:7851862..7991750hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38139889
hg19139889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4785n223
Supporting Variantsnssv18105243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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