A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578189



Internal ID16018912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1007994..1013149hg38UCSC Ensembl
Innerchr19:1007993..1013148hg19UCSC Ensembl
Innerchr19:958993..964148hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385156
hg195156
hg185156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891282
Samples
Known GenesGRIN3B, TMEM259
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578189
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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