A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578188



Internal ID16018911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:923744..1059005hg38UCSC Ensembl
Innerchr19:923744..1059004hg19UCSC Ensembl
Innerchr19:874744..1010004hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38135262
hg19135261
hg18135261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891281
Samples
Known GenesABCA7, ARID3A, CNN2, GRIN3B, TMEM259, WDR18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578188
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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