A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936951



Internal ID21357020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88652397..88652494hg38UCSC Ensembl
chr15:89195628..89195725hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183978
SamplesHG002
Known GenesISG20
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936951
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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