A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922766



Internal ID22697991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32493640..32493946hg38UCSC Ensembl
chr7:32533252..32533558hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435384
Samples
Known GenesLSM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922766
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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