A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411292



Internal ID21068845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67004178..67007346hg38UCSC Ensembl
chr5:66300006..66303174hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg383169
hg193169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133936
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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