A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699387



Internal ID21221232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143015717..143015803hg38UCSC Ensembl
chr8:144097134..144097220hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816168
Supporting Variants
Samples
Known GenesLOC100133669
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699387
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.333333


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