A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112164



Internal ID21295430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24120919..24292632hg38UCSC Ensembl
Innerchr19:24303721..24475434hg19UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38171714
hg19171714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101354
Samplessample302
Known GenesHAVCR1P1, ZNF254
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112164
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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