A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066021



Internal ID19155240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42811447..43252073hg38UCSC Ensembl
Innerchr19:43315599..43756225hg19UCSC Ensembl
Innerchr19:48007439..48448065hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38440627
hg19440627
hg18440627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3566n100
Supporting Variantsnssv3722981
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066021
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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