A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202736



Internal ID20769776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22855891..22934229hg38UCSC Ensembl
chr1:23182384..23260722hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3878339
hg1978339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330032
Supporting Variants
Samples
Known GenesEPHB2, MIR4253
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202736
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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