A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502651



Internal ID20875897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9881368..9881675hg38UCSC Ensembl
chr17:9784685..9784992hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039172
Samples
Known GenesGLP2R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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