A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919875



Internal ID22695098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1582727..1583923hg38UCSC Ensembl
chr7:1622363..1623559hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429686
Samples
Known GenesPSMG3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919875
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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