A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123718



Internal ID19253503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184721934..184722026hg38UCSC Ensembl
Outerchr3:184439722..184439814hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956665, nssv3974694
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123718
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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