A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136362



Internal ID18911443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50674569..50675469hg38UCSC Ensembl
Outerchr3:50712000..50712900hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989985
SamplesKWS2
Known GenesDOCK3, MIR4787
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136362
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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