A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148617



Internal ID19201854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:38575705..38631869hg38UCSC Ensembl
Outerchr10:38868799..38925000hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3856165
hg1956202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000655
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148617
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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