A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057292



Internal ID19146511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24219440..24413936hg38UCSC Ensembl
Innerchr19:24402242..24596738hg19UCSC Ensembl
Innerchr19:24194082..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38194497
hg19194497
hg18194497
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3483n100
Supporting Variantsnssv3570693, nssv3570692, nssv3570695, nssv3570694, nssv3570696
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)nsv1057292
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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