A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226506



Internal ID22369283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:97434100..97468266hg38UCSC Ensembl
Outerchr7:97063412..97097578hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3834167
hg1934167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277422, nssv14277421
SamplesHG00731, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226506
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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