A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14276643



Internal ID22262433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:31963430..31977388hg38UCSC Ensembl
Outerchr10:32252358..32266316hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3813959
hg1913959
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225311
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14276643
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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