A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346517



Internal ID21004070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167046347..167046776hg38UCSC Ensembl
chr2:167902857..167903286hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080273
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346517
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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