A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134897



Internal ID18923424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:75809018..75822618hg38UCSC Ensembl
Outerchr7:75438336..75451936hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3813601
hg1913601
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988385
SamplesKWS1
Known GenesCCL24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134897
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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