A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348367



Internal ID21005920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167077048..167077398hg38UCSC Ensembl
chr2:167933558..167933908hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207361
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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