A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919879



Internal ID22695102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99156611..99191243hg38UCSC Ensembl
chr7:98754234..98788866hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3834633
hg1934633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444935
Samples
Known GenesKPNA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919879
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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