A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061024



Internal ID18803555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55655735..55705993hg38UCSC Ensembl
Innerchr19:56167101..56217359hg19UCSC Ensembl
Innerchr19:60858913..60909171hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3850259
hg1950259
hg1850259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570431
Samples
Known GenesEPN1, U2AF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061024
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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