A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185151



Internal ID20752191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4249227..4256557hg38UCSC Ensembl
chr10:4291419..4298749hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg387331
hg197331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449205
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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