A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200121



Internal ID20767161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13985052..14044906hg38UCSC Ensembl
chr1:14311547..14371401hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3859855
hg1959855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00033


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