A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375792



Internal ID22601461
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 StatusS
Merged Variantsnsv5929605
Supporting Variants
Samples
Known GenesMYH10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375792
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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