A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187336



Internal ID20754376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57456997..57595109hg38UCSC Ensembl
chr10:59216757..59354869hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38138113
hg19138113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187336
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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