A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195265



Internal ID21334176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60365042..60365042hg38UCSC Ensembl
chr15:60657241..60657241hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951873
Supporting Variants
SamplesHG002
Known GenesANXA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195265
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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