A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063837



Internal ID19153056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46193259..46257769hg38UCSC Ensembl
Innerchr19:46696516..46761026hg19UCSC Ensembl
Innerchr19:51388356..51452866hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3864511
hg1964511
hg1864511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3607n100
Supporting Variantsnssv3573802
Samples
Known GenesDKFZp434J0226, IGFL1, RNU6-66P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063837
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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