A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188355



Internal ID20755395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26803910..27303927hg38UCSC Ensembl
chr10:27092839..27592856hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38500018
hg19500018
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436760
Supporting Variants
Samples
Known GenesABI1, ACBD5, ANKRD26, LINC00202-1, LRRC37A6P, MASTL, YME1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188355
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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