A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941483



Internal ID21361552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64371908..64372027hg38UCSC Ensembl
chr15:64664107..64664226hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184624
SamplesHG002
Known GenesKIAA0101
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941483
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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