A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385943



Internal ID22239056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34854675..34855873hg38UCSC Ensembl
chr17:33181694..33182892hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558792
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385943
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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