A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415557



Internal ID21073110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120909703..121179937hg38UCSC Ensembl
chr5:120245398..120515632hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38270235
hg19270235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5919n223
Supporting Variantsnssv18124767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415557
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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