A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446272



Internal ID21103825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119109755..119114192hg38UCSC Ensembl
chr10:120869267..120873704hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384438
hg194438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979596
Samples
Known GenesFAM45A, FAM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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