A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339760



Internal ID20997313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189687208..189687763hg38UCSC Ensembl
chr2:190551934..190552489hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083224
Samples
Known GenesANKAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339760
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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