A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192762



Internal ID20759802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72689801..72695000hg38UCSC Ensembl
chr10:74449559..74454758hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450794
Supporting Variants
Samples
Known GenesMCU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192762
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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