A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080469



Internal ID20647510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173387165..173388981hg38UCSC Ensembl
chr2:174251893..174253709hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355311
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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