A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14277809



Internal ID22198918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156142885..156157684hg38UCSC Ensembl
Outerchr7:155935579..155950378hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3814800
hg1914800
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212974
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14277809
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer