A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432242



Internal ID21394244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62413897..62415593hg38UCSC Ensembl
chr15:62706096..62707792hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381697
hg191697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv260n172
Supporting Variantsnssv15749669, nssv15751734, nssv15752936, nssv15753115, nssv15749164, nssv15750699, nssv15751745, nssv15753295, nssv15750955
SamplesNB12, SMI034, BTQ038, NB10, BTQ055, BTQ016, SMI041, NB11, SMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432242
Frequency
Sample Size15
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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