A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124782



Internal ID19270769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:27240892..27250792hg38UCSC Ensembl
Outerchr19:27731800..27741700hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg389901
hg199901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1750n106
Supporting Variantsnssv3976835
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124782
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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