A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913632



Internal ID22688848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131773478..131775983hg38UCSC Ensembl
chr7:131458237..131460742hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg382506
hg192506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913632
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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