A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400499



Internal ID21058052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76357255..76362625hg38UCSC Ensembl
chr5:75653080..75658450hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg385371
hg195371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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