A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037516



Internal ID18780047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94647754..94757047hg38UCSC Ensembl
Innerchr10:96407511..96516804hg19UCSC Ensembl
Innerchr10:96397501..96506794hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38109294
hg19109294
hg18109294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv955n100
Supporting Variantsnssv3505059
Samples
Known GenesCYP2C18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037516
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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