A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062392



Internal ID19151611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57019563..57122783hg38UCSC Ensembl
Innerchr19:57530931..57634151hg19UCSC Ensembl
Innerchr19:62222743..62325963hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38103221
hg19103221
hg18103221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570449
Samples
Known GenesUSP29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062392
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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