A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929340



Internal ID21349409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81056794..81056794hg38UCSC Ensembl
chr17:79030594..79030594hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185094
SamplesHG002
Known GenesBAIAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929340
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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