A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202492



Internal ID20769532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23722648..23724446hg38UCSC Ensembl
chr1:24049138..24050936hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381799
hg191799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315881
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202492
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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