A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944406



Internal ID21364475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8746874..8746874hg38UCSC Ensembl
chr17:8650192..8650192hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184402
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944406
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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