A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753931



Internal ID21384302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61228538..61229410hg38UCSC Ensembl
chr15:61520737..61521609hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432240
Supporting Variants
SamplesBTQ016
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753931
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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