A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14264202



Internal ID22257591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:36316505..37269269hg38UCSC Ensembl
Outerchr19:36807407..37760171hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38139180
hg19139180
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3245329
Supporting Variants
SamplesNA19238
Known GenesLINC00665, LOC284412, LOC644189, LOC728752, ZFP14, ZFP82, ZNF260, ZNF345, ZNF382, ZNF383, ZNF420, ZNF461, ZNF529, ZNF566, ZNF567, ZNF568, ZNF585A, ZNF585B, ZNF790, ZNF790-AS1, ZNF829, ZNF850
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14264202
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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