A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573778



Internal ID18872059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43421138..43453235hg38UCSC Ensembl
Innerchr19:43925290..43957387hg19UCSC Ensembl
Innerchr19:48617130..48649227hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3832098
hg1932098
hg1832098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058848
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573778
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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