A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338560



Internal ID22260566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149227675..149228110hg38UCSC Ensembl
chr7:148924766..148925201hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225472
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338560
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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