A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085525



Internal ID20652565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219690081..219691808hg38UCSC Ensembl
chr2:220554803..220556530hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381728
hg191728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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