A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222661



Internal ID22366667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:86819642..86881589hg38UCSC Ensembl
Outerchr7:86448958..86510905hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3861948
hg1961948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277415
SamplesHG00731
Known GenesGRM3, KIAA1324L
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222661
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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