A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940528



Internal ID21360597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9882986..9883035hg38UCSC Ensembl
chr17:9786303..9786352hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176248
SamplesHG002
Known GenesGLP2R
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940528
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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