A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926737



Internal ID22701964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78076547..78076877hg38UCSC Ensembl
chr7:77705864..77706194hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449313
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926737
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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