A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200822



Internal ID20767862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14627628..14891723hg38UCSC Ensembl
chr1:14954124..15218219hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38264096
hg19264096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330944
Supporting Variants
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200822
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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