A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687449



Internal ID21209306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166755887..166761921hg38UCSC Ensembl
chr4:167677038..167683072hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386035
hg196035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809800
Supporting Variants
Samples
Known GenesSPOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687449
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.75


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