A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432240



Internal ID21394242
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 StatusM
Merged Variantsdgv259n172
Supporting Variantsnssv15752783, nssv15753931
SamplesBTQ016, SMI018
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432240
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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