A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927537



Internal ID21347606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60552153..60552153hg38UCSC Ensembl
chr17:58629514..58629514hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184424
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927537
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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