A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125867



Internal ID19264765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:1291561..1291667hg38UCSC Ensembl
Outerchr6:1291796..1291902hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3964084, nssv3979907
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125867
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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