A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062653



Internal ID19151872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39633228..39672601hg38UCSC Ensembl
Innerchr19:40123868..40163241hg19UCSC Ensembl
Innerchr19:44815708..44855081hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3839374
hg1939374
hg1839374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568206
Samples
Known GenesLGALS16, LOC100129935
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062653
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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