A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055900



Internal ID18798431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12979147..13034197hg38UCSC Ensembl
Innerchr19:13089961..13145011hg19UCSC Ensembl
Innerchr19:12950961..13006011hg18UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg3855051
hg1955051
hg1855051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564774
Samples
Known GenesNFIX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055900
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