A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063725



Internal ID18806256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48238810..48264769hg38UCSC Ensembl
Innerchr19:48742067..48768026hg19UCSC Ensembl
Innerchr19:53433879..53459838hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3825960
hg1925960
hg1825960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3615n100
Supporting Variantsnssv3574957, nssv3574958
Samples
Known GenesCARD8, LOC100505812
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063725
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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