A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14277872



Internal ID22198930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:1239410..1277783hg38UCSC Ensembl
Outerchr7:1279046..1317419hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383649
hg193649
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223383
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14277872
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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