A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208376



Internal ID20775416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238539201..238543200hg38UCSC Ensembl
chr2:239447842..239451841hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350595
Supporting Variants
Samples
Known GenesLINC01107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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