A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747998



Internal ID21389349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95148033..95149304hg38UCSC Ensembl
chr15:95691262..95692533hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432280
Supporting Variants
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747998
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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