A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089479



Internal ID20656519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61481559..61481848hg38UCSC Ensembl
chr2:61708694..61708983hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354644
Supporting Variants
Samples
Known GenesXPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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