A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910215



Internal ID22685425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99454134..99456428hg38UCSC Ensembl
chr7:99051757..99054051hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382295
hg192295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430529
Samples
Known GenesATP5J2-PTCD1, CPSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910215
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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