A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432280



Internal ID21394282
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 StatusM
Merged Variants
Supporting Variantsnssv15747998
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432280
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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