A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144544



Internal ID19279816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:190237605..190237921hg38UCSC Ensembl
Outerchr3:189955394..189955710hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2658n106
Supporting Variantsnssv3995374
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144544
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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