A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3555n71



Internal ID6321175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:789890..1410493hg19UCSC Ensembl
chr19:740890..1361493hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv910322, nsv910311
SamplesIS37172, IS32737
Known GenesABCA7, ARID3A, ATP5D, AZU1, C19orf22, C19orf23, C19orf24, C19orf26, C19orf6, CFD, CIRBP, CNN2, DAZAP1, EFNA2, ELANE, GAMT, GPX4, GRIN3B, HMHA1, KISS1R, LPPR3, MED16, MIDN, MIR3187, MIR4745, MUM1, NDUFS7, POLR2E, PRTN3, PTBP1, SBNO2, STK11, WDR18
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3555n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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