A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708582



Internal ID21230370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126417905..126418218hg38UCSC Ensembl
chr10:128106474..128106787hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789112
Supporting Variants
Samples
Known GenesLINC00601
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708582
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.890625


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