A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338785



Internal ID22227757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155886349..155886418hg38UCSC Ensembl
chr7:155679043..155679112hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218425
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338785
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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