A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110463



Internal ID19270436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168714370..168716261hg38UCSC Ensembl
Outerchr6:169114600..169116400hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381892
hg191801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960114
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110463
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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