A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061778



Internal ID19150997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43044850..43124678hg38UCSC Ensembl
Innerchr19:43549002..43628830hg19UCSC Ensembl
Innerchr19:48240842..48320670hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3879829
hg1979829
hg1879829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723064
Samples
Known GenesPSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061778
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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