A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917498



Internal ID22692717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6097832..6099455hg38UCSC Ensembl
chr7:6137463..6139086hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917498
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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