A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338592



Internal ID20996145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18138840..18143502hg38UCSC Ensembl
chr2:18320106..18324768hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg384663
hg194663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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