A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355467



Internal ID22195759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18268816..18268870hg38UCSC Ensembl
chr11:18290363..18290417hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528037
Supporting Variants
SamplesHG00731
Known GenesSAA1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355467
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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