A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336990



Internal ID20994543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142551301..142556600hg38UCSC Ensembl
chr2:143308870..143314169hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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