A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455009



Internal ID21112562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24950201..24953300hg38UCSC Ensembl
chr10:25239130..25242229hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979272
Samples
Known GenesPRTFDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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