A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432225



Internal ID21394227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41657059..41657600hg38UCSC Ensembl
chr15:41949257..41949798hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv257n172
Supporting Variantsnssv15750545, nssv15751088
SamplesBTQ038, BTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432225
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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