A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402142



Internal ID21059695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87142040..87146446hg38UCSC Ensembl
chr5:86437857..86442263hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg384407
hg194407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136103
Samples
Known GenesLOC101929380
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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