A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908235



Internal ID22683445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70163018..70164923hg38UCSC Ensembl
chr10:71922774..71924679hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381906
hg191906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357546
Samples
Known GenesSAR1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908235
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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