A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578676



Internal ID16019399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14621589..14626619hg38UCSC Ensembl
Innerchr19:14732401..14737431hg19UCSC Ensembl
Innerchr19:14593401..14598431hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385031
hg195031
hg185031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv894903, nssv894904
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578676
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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