A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401281



Internal ID21058834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74437355..74442787hg38UCSC Ensembl
chr5:73733180..73738612hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg385433
hg195433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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