A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340118



Internal ID20997671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159860087..159860690hg38UCSC Ensembl
chr2:160716598..160717201hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080510
Samples
Known GenesLY75, LY75-CD302
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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