A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981406



Internal ID20548446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3058401..3259500hg38UCSC Ensembl
chr10:3100593..3301692hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38201100
hg19201100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437272
Supporting Variants
Samples
Known GenesPFKP, PITRM1, PITRM1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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