A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917464



Internal ID22692683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74449479..74450479hg38UCSC Ensembl
chr7:73863809..73864809hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917464
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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