A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344739



Internal ID21002292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97681952..97688510hg38UCSC Ensembl
chr2:98298415..98304973hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg386559
hg196559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091657
Samples
Known GenesLINC01125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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