A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455282



Internal ID21112835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3085901..3154200hg38UCSC Ensembl
chr10:3128093..3196392hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3868300
hg1968300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981418
Samples
Known GenesPFKP, PITRM1, PITRM1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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