A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703449



Internal ID21225260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81669286..81669376hg38UCSC Ensembl
chr16:81702891..81702981hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795607
Supporting Variants
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703449
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.833333


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