A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351795



Internal ID21009348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239281521..239314200hg38UCSC Ensembl
chr2:240203217..240235895hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3832680
hg1932679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208382
Samples
Known GenesHDAC4, MIR4269
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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