A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230011



Internal ID22371670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71803814..71804205hg38UCSC Ensembl
chr16:71837717..71838108hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381538, nssv14379367
SamplesNA19240, HG00513
Known GenesAP1G1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3230011
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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