A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085815



Internal ID20652855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217215901..217224700hg38UCSC Ensembl
chr2:218080624..218089423hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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