A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897355



Internal ID172391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15358943..15442510hg38UCSC Ensembl
chr1:15685439..15769006hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3883568
hg1983568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417732
Supporting Variants
Samples
Known GenesCTRC, EFHD2, FHAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897355
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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