A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753829



Internal ID21393021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31324798..31368797hg38UCSC Ensembl
chr15:31617001..31661000hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3844000
hg1944000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432204
Supporting Variants
SamplesSMI041
Known GenesKLF13
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753829
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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