A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930651



Internal ID21350720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57606185..57606185hg38UCSC Ensembl
chr1:58071857..58071857hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193547
SamplesHG002
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930651
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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