A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746348



Internal ID21393042
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 StatusS
Merged Variantsnsv4432278
Supporting Variants
SamplesSMI041
Known GenesCHD2, LOC100507217, MIR3175
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746348
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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