A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344959



Internal ID21002512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231451193..231452516hg38UCSC Ensembl
chr2:232315904..232317227hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381324
hg191324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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