A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115761



Internal ID19256055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:136094452..136098852hg38UCSC Ensembl
Outerchr7:135779200..135783600hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg384401
hg194401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977568
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115761
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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