A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125671



Internal ID19286010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:33249758..33250371hg38UCSC Ensembl
Outerchr19:33740664..33741277hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1770n106
Supporting Variantsnssv3983879
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125671
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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