A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184281



Internal ID21323077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88077037..88077037hg38UCSC Ensembl
chr16:88110643..88110643hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941634
Supporting Variants
SamplesHG002
Known GenesBANP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184281
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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