A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564760



Internal ID22433487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131868491..131868491hg38UCSC Ensembl
chr7:131553250..131553250hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338321, nssv14338322
SamplesHG00512, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564760
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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