A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089128



Internal ID20656168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38171772..38175791hg38UCSC Ensembl
chr2:38398914..38402933hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg384020
hg194020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345614
Supporting Variants
Samples
Known GenesCYP1B1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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