A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192772



Internal ID22343309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35070025..35070510hg38UCSC Ensembl
chr6:35037802..35038287hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325555, nssv14325556
SamplesHG00731, HG00733
Known GenesANKS1A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192772
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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