A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402536



Internal ID21060089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75780095..75882808hg38UCSC Ensembl
chr5:75075920..75178633hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38102714
hg19102714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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