A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399802



Internal ID21057355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97007041..97007594hg38UCSC Ensembl
chr5:96342745..96343298hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135694
Samples
Known GenesLNPEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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