A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501028



Internal ID20874258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27881264..27883837hg38UCSC Ensembl
chr17:26208290..26210863hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382574
hg192574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034534
Samples
Known GenesLYRM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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