A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568812



Internal ID18520407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42758818..42833322hg38UCSC Ensembl
Innerchr19:43262970..43337474hg19UCSC Ensembl
Innerchr19:47954810..48029314hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3874505
hg1974505
hg1874505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055222
Supporting Variants
Samples
Known GenesLOC100289650, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568812
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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