A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406677



Internal ID21064230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87205901..87207000hg38UCSC Ensembl
chr5:86501718..86502817hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136112
Samples
Known GenesLOC101929380
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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