A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110326



Internal ID18938783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:38602460..38603360hg38UCSC Ensembl
Outerchr19:39093100..39094000hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1780n106
Supporting Variantsnssv3959974
SamplesKWS1
Known GenesMAP4K1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110326
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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