A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529608



Internal ID22399000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166585488..166586678hg38UCSC Ensembl
chr6:166998976..167000166hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8213n152
Supporting Variantsnssv14332146, nssv14332144, nssv14332145
SamplesNA19238, NA19239, NA19240
Known GenesRPS6KA2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529608
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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