A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921774



Internal ID22696998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74245723..74246205hg38UCSC Ensembl
chr7:73660053..73660535hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430185
Samples
Known GenesRFC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921774
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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