A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578292



Internal ID16019015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1466625..1470585hg38UCSC Ensembl
Innerchr19:1466624..1470584hg19UCSC Ensembl
Innerchr19:1417624..1421584hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383961
hg193961
hg183961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6201n54
Supporting Variantsnssv891803
Samples
Known GenesAPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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