A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191213



Internal ID21330073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26564036..26564036hg38UCSC Ensembl
chr10:26852965..26852965hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944730
Supporting Variants
SamplesHG002
Known GenesAPBB1IP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191213
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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