A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929605



Internal ID22704861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8496427..8496595hg38UCSC Ensembl
chr17:8399745..8399913hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375792
Samples
Known GenesMYH10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929605
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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