A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447616



Internal ID21105169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3063695..3087235hg38UCSC Ensembl
chr10:3105887..3129427hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3823541
hg1923541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981411
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447616
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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