A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401691



Internal ID21059244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74042142..74042665hg38UCSC Ensembl
chr5:73337967..73338490hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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