A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922512



Internal ID22697737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73244314..73244401hg38UCSC Ensembl
chr10:75004072..75004159hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357181
Samples
Known GenesDNAJC9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922512
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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