A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432244



Internal ID21394246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62413968..62415690hg38UCSC Ensembl
chr15:62706167..62707889hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381723
hg191723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv260n172
Supporting Variantsnssv15747888
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432244
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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