A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208356



Internal ID20775396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237250912..237263156hg38UCSC Ensembl
chr2:238159555..238171799hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3812245
hg1912245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208356
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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