A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922831



Internal ID22698056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23194631..23194957hg38UCSC Ensembl
chr7:23234250..23234576hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444299
Samples
Known GenesNUPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922831
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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