A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403915



Internal ID21061468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117528289..117867719hg38UCSC Ensembl
chr5:116863984..117203414hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38339431
hg19339431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122850
Samples
Known GenesLINC00992, LOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403915
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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