A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060069



Internal ID19149288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34045547..34163064hg38UCSC Ensembl
Innerchr19:34536452..34653969hg19UCSC Ensembl
Innerchr19:39228292..39345809hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38117518
hg19117518
hg18117518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566584
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060069
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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