A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091868



Internal ID20658908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8908065..8908665hg38UCSC Ensembl
chr2:9048195..9048795hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339949
Supporting Variants
Samples
Known GenesMBOAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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