A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115734



Internal ID19250044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170740812..170745912hg38UCSC Ensembl
Outerchr6:171049900..171055000hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977541
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115734
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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