A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180356



Internal ID20747396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56559601..56562000hg38UCSC Ensembl
chr13:57133735..57136134hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479487
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180356
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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