A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077877



Internal ID20644918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135176173..135180067hg38UCSC Ensembl
chr2:135933743..135937637hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg383895
hg193895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354847
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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