A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634910



Internal ID21583215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102611779..102611779hg38UCSC Ensembl
chr7:102252226..102252226hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142218
SamplesHG00731
Known GenesRASA4, RASA4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634910
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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