A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193461



Internal ID20760501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102822626..102957863hg38UCSC Ensembl
chr14:103288963..103424200hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38135238
hg19135238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496729
Supporting Variants
Samples
Known GenesAMN, CDC42BPB, TRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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