A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746749



Internal ID21386533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43226954..43305638hg38UCSC Ensembl
chr17:41379001..41383000hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3878685
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432526
Supporting Variants
SamplesMDQ025
Known GenesLINC00854
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746749
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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