A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081246



Internal ID20648286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165695101..165698900hg38UCSC Ensembl
chr2:166551611..166555410hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342410
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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