A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141510



Internal ID19251199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26673372..26712071hg38UCSC Ensembl
Outerchr6:26673600..26712300hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3838700
hg1938701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993016
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141510
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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