A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408334



Internal ID21065887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91617257..91617727hg38UCSC Ensembl
chr5:90913074..90913544hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408334
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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