A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753263



Internal ID20529123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102611778..102611778hg38UCSC Ensembl
chr7:102252225..102252225hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277907
Samples
Known GenesRASA4, RASA4B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753263
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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