A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051556



Internal ID18794087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113017050..113207934hg38UCSC Ensembl
Innerchr13:113671364..113862248hg19UCSC Ensembl
Innerchr13:112719365..112910249hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38190885
hg19190885
hg18190885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525617
Samples
Known GenesF10, F7, MCF2L, PCID2, PROZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051556
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