A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698625



Internal ID21220484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88652385..88652445hg38UCSC Ensembl
chr15:89195616..89195676hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795515
Supporting Variants
Samples
Known GenesISG20
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698625
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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