A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908655



Internal ID22683865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75043939..75048248hg38UCSC Ensembl
chr10:76803697..76808006hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg384310
hg194310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353549
Samples
Known GenesDUPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908655
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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