A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225652



Internal ID22368718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33311924..33311975hg38UCSC Ensembl
chr11:33333470..33333521hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357604
SamplesNA19239
Known GenesHIPK3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225652
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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