A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124931



Internal ID19269936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:181292999..181320299hg38UCSC Ensembl
Outerchr5:180720000..180747300hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3827301
hg1927301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977737
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124931
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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