A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935580



Internal ID21355650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65326077..65326473hg38UCSC Ensembl
chr15:65618415..65618811hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183271
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935580
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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