A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129767



Internal ID19277760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:150269028..150269113hg38UCSC Ensembl
Outerchr6:150590164..150590249hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3964101
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129767
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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