A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151058



Internal ID18853950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100950765..100962777hg38UCSC Ensembl
Outerchr7:100548399..100554600hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3812013
hg196202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001991
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151058
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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