A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188255



Internal ID20755295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2846098..3581354hg38UCSC Ensembl
chr10:2888290..3623546hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38735257
hg19735257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442520
Supporting Variants
Samples
Known GenesPFKP, PITRM1, PITRM1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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