A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14261996



Internal ID22257008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:81241578..81290787hg38UCSC Ensembl
Outerchr17:79215378..79264587hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381654
hg191654
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3245102
Supporting Variants
SamplesNA19238
Known GenesSLC38A10
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14261996
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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