A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153775



Internal ID18852343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126534986..126535111hg38UCSC Ensembl
Outerchr3:126253829..126253954hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002428
SamplesKWB1
Known GenesCHST13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153775
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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