A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv894903



Internal ID15842173
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 StatusS
Merged Variantsnsv578676
Supporting Variants
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv894903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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