A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371304



Internal ID22596973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18127207..18127857hg38UCSC Ensembl
chr17:18030521..18031171hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944310
Supporting Variants
Samples
Known GenesMYO15A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371304
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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