A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14378620



Internal ID22208744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36088877..36195491hg38UCSC Ensembl
chr17:34416223..34522890hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38106615
hg19106668
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3557940
Supporting Variants
SamplesHG00732
Known GenesCCL3, CCL3L1, CCL3L3, CCL4, TBC1D3B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14378620
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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