A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201243



Internal ID22350579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99490127..99490383hg38UCSC Ensembl
chr7:99087750..99088006hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335656
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201243
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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