A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354452



Internal ID21012005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173697926..173698381hg38UCSC Ensembl
chr2:174562654..174563109hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354452
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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