A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411591



Internal ID21069144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164455733..164456179hg38UCSC Ensembl
chr5:163882739..163883185hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127621
Samples
Known GenesLOC101927835
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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