A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252610



Internal ID22263035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69593817..69631604hg38UCSC Ensembl
Outerchr10:71353573..71391360hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3232660
Supporting Variants
SamplesNA19238
Known GenesC10orf35
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14252610
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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