A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703943



Internal ID127609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69164424..69164475hg38UCSC Ensembl
chr15:69456763..69456814hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144343
Supporting Variants
Samples
Known GenesGLCE, MIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703943
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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