A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14253802



Internal ID22186326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124506089..124530666hg38UCSC Ensembl
Outerchr10:126194658..126219235hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381880
hg191880
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3242538
Supporting Variants
SamplesHG00731
Known GenesLHPP
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14253802
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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