A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330609



Internal ID22201764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161181351..161186150hg38UCSC Ensembl
chr6:161602383..161607182hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206765
Supporting Variants
SamplesHG00732
Known GenesAGPAT4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330609
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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