A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183034



Internal ID20750074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61695486..61695826hg38UCSC Ensembl
chr10:63455244..63455584hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449747
Supporting Variants
Samples
Known GenesC10orf107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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