A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390708



Internal ID21048261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38070280..38145752hg38UCSC Ensembl
chr5:38070382..38145854hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3875473
hg1975473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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