A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325643



Internal ID22206343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37728325..37728325hg38UCSC Ensembl
chr6:37696101..37696101hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564655
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325643
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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