A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507622



Internal ID20880916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17483859..17490307hg38UCSC Ensembl
chr17:17387173..17393621hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg386449
hg196449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034655
Samples
Known GenesMED9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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