A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410122



Internal ID21067675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155421205..155421728hg38UCSC Ensembl
chr5:154800765..154801288hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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