A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329608



Internal ID22192328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121380638..121380908hg38UCSC Ensembl
chr6:121701784..121702054hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529914
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329608
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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