A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133564



Internal ID19265549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:171620610..171622310hg38UCSC Ensembl
Outerchr3:171338400..171340100hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969128
SamplesKWS2
Known GenesPLD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133564
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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