A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935705



Internal ID21355775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81323239..81323317hg38UCSC Ensembl
chr15:81615580..81615658hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183426
SamplesHG002
Known GenesSTARD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935705
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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