A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909614



Internal ID22684824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99586538..99586913hg38UCSC Ensembl
chr7:99184161..99184536hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909614
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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