A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125921



Internal ID19269494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:131868491..131868713hg38UCSC Ensembl
Outerchr7:131553250..131553472hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980048, nssv3963437
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125921
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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