A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379367



Internal ID22313672
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230011
Supporting Variants
SamplesNA19240
Known GenesAP1G1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379367
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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