A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708150



Internal ID21229943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9273070..9273268hg38UCSC Ensembl
chr10:9315033..9315231hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708150
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.625


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