A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091836



Internal ID20658876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88748504..88748848hg38UCSC Ensembl
chr2:89048021..89048365hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340410
Supporting Variants
Samples
Known GenesRPIA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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