A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911423



Internal ID22686637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23187899..23187950hg38UCSC Ensembl
chr7:23227518..23227569hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443569
Samples
Known GenesNUPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911423
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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