A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078628



Internal ID20645669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141407814..141520856hg38UCSC Ensembl
chr2:142165383..142278425hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38113043
hg19113043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340659
Supporting Variants
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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