A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578693



Internal ID16366102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14934576..14936904hg38UCSC Ensembl
Innerchr19:15045388..15047716hg19UCSC Ensembl
Innerchr19:14906388..14908716hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382329
hg192329
hg182329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6282n54
Supporting Variantsnssv894944
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578693
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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