A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932563



Internal ID21352632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894052..39894052hg38UCSC Ensembl
chr15:40186253..40186253hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194585
SamplesHG002
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932563
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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