A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181220



Internal ID20748260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68073901..68109000hg38UCSC Ensembl
chr10:69833658..69868757hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3835100
hg1935100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453440
Supporting Variants
Samples
Known GenesHERC4, MYPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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