A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358629



Internal ID22210958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77823215..77823622hg38UCSC Ensembl
chr11:77534261..77534668hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213148
Supporting Variants
SamplesHG00732
Known GenesAAMDC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358629
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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