A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681086



Internal ID21202946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59697012..59697139hg38UCSC Ensembl
chr10:61456770..61456897hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790116
Supporting Variants
Samples
Known GenesSLC16A9
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681086
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.517241


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