A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038480



Internal ID19127699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63297894..63439731hg38UCSC Ensembl
Innerchr13:63872027..64013864hg19UCSC Ensembl
Innerchr13:62770028..62911865hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38141838
hg19141838
hg18141838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526604
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)nsv1038480
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