A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14311236



Internal ID22204832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:869568..869633hg38UCSC Ensembl
chr4:863356..863421hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202346
Supporting Variants
SamplesHG00732
Known GenesGAK
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14311236
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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