A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177474



Internal ID20744514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70852105..70863375hg38UCSC Ensembl
chr13:71426237..71437507hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3811271
hg1911271
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177474
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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