A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210658



Internal ID22358489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:52016369..52054976hg38UCSC Ensembl
Outerchr7:52084065..52122672hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3838608
hg1938608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277785
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210658
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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