A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066166



Internal ID18808697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42764459..42835356hg38UCSC Ensembl
Innerchr19:43268611..43339508hg19UCSC Ensembl
Innerchr19:47960451..48031348hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3870898
hg1970898
hg1870898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3554n100
Supporting Variantsnssv3568862
Samples
Known GenesLOC100289650, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066166
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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