A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152063



Internal ID18854605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46215763..46262664hg38UCSC Ensembl
Outerchr10:47586999..47633900hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3846902
hg1946902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999246
SamplesKWB1
Known GenesANTXRLP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152063
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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