A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412349



Internal ID21069902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87164011..87164761hg38UCSC Ensembl
chr5:86459828..86460578hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136107
Samples
Known GenesLOC101929380
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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