A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087724



Internal ID20654764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228468937..228493073hg38UCSC Ensembl
chr2:229333653..229357789hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3824137
hg1924137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087724
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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