A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199295



Internal ID20766335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113173601..113251012hg38UCSC Ensembl
chr1:113716223..113793634hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3877412
hg1977412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331428
Supporting Variants
Samples
Known GenesLOC643441
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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