A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115725



Internal ID19267679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:113531498..113536798hg38UCSC Ensembl
Outerchr6:113852700..113858000hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385301
hg195301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977533
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115725
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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