A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208639



Internal ID22356843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113086157..113086444hg38UCSC Ensembl
chr7:112726212..112726499hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14337700, nssv14337699
SamplesHG00513, HG00514
Known GenesGPR85
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208639
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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