A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139660



Internal ID19260101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:65552697..65557297hg38UCSC Ensembl
Outerchr16:65586600..65591200hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384601
hg194601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977246
SamplesKWS2
Known GenesLINC00922
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139660
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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