A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202444



Internal ID20769484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36392144..36392851hg38UCSC Ensembl
chr1:36857745..36858452hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202444
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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