A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148806



Internal ID19196625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155957705..155959806hg38UCSC Ensembl
Outerchr7:155750399..155752500hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382102
hg192102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997593
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148806
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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