A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913584



Internal ID22688800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142328666..142349543hg38UCSC Ensembl
chr7:142028490..142048000hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3820878
hg1919511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913584
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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