A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056401



Internal ID18798932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9031263..9161005hg38UCSC Ensembl
Innerchr19:9141939..9271681hg19UCSC Ensembl
Innerchr19:9002939..9132681hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38129743
hg19129743
hg18129743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564686
Samples
Known GenesOR1M1, OR7G1, OR7G2, OR7G3, ZNF317
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056401
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