A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944083



Internal ID21364152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77776492..77776492hg38UCSC Ensembl
chr17:75772574..75772574hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185755
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944083
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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