A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399655



Internal ID21057208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98739835..98740161hg38UCSC Ensembl
chr5:98075539..98075865hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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