A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506996



Internal ID20880284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32698424..32699175hg38UCSC Ensembl
chr17:31025442..31026193hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035583
Samples
Known GenesMYO1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer