A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351299



Internal ID21008852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17844550..17844834hg38UCSC Ensembl
chr2:18025817..18026101hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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