A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592984



Internal ID16380393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195269634..195271115hg38UCSC Ensembl
Innerchr3:194990363..194991844hg19UCSC Ensembl
Innerchr3:196471652..196473133hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381482
hg191482
hg181482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv986722, nssv986721
Samples
Known GenesXXYLT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592984
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer