A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010491



Internal ID21919834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102606517..102606786hg38UCSC Ensembl
chr7:102246964..102247233hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558371
Samples
Known GenesRASA4, RASA4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010491
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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