A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398017



Internal ID21055570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134735781..134738063hg38UCSC Ensembl
chr5:134071471..134073753hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382283
hg192283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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