A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118584



Internal ID19252380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:74359702..74399402hg38UCSC Ensembl
Outerchr16:74393600..74433300hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3839701
hg1939701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959096
SamplesKWS1
Known GenesLOC283922
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118584
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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