A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412827



Internal ID21070380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58121917..58122767hg38UCSC Ensembl
chr5:57417744..57418594hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133639
Samples
Known GenesLOC101928569
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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