A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405049



Internal ID21062602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64025501..64028600hg38UCSC Ensembl
chr5:63321328..63324427hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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