A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331724



Internal ID22235285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117459392..117459490hg38UCSC Ensembl
chr6:117780555..117780653hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528910
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331724
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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