A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156029



Internal ID22086534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155631522..155641984hg38UCSC Ensembl
Outerchr3:155625941..155643593hg38UCSC Ensembl
Innerchr3:155349311..155359773hg19UCSC Ensembl
Outerchr3:155343730..155361382hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3817653
hg1917653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015927
Samples
Known GenesPLCH1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156029
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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