A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3574958



Internal ID18526553
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 StatusS
Merged Variantsnsv1063725
Supporting Variants
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)nssv3574958
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