A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724902



Internal ID18676497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47260028..47307644hg38UCSC Ensembl
Innerchr19:47763285..47810901hg19UCSC Ensembl
Innerchr19:52455125..52502741hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3847617
hg1947617
hg1847617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059583
Supporting Variants
Samples
Known GenesCCDC9, PRR24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3724902
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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