A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432278



Internal ID21394280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92879771..92915770hg38UCSC Ensembl
chr15:93423001..93459000hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3836000
hg1936000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746348
SamplesSMI041
Known GenesCHD2, LOC100507217, MIR3175
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432278
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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