A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066290



Internal ID19155509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42798345..43065876hg38UCSC Ensembl
Innerchr19:43302497..43570028hg19UCSC Ensembl
Innerchr19:47994337..48261868hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38267532
hg19267532
hg18267532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3556n100
Supporting Variantsnssv3569557
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, 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)nsv1066290
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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