A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929224



Internal ID21349293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127392028..127392028hg38UCSC Ensembl
chr10:129190292..129190292hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190702
SamplesHG002
Known GenesDOCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929224
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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