A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043400



Internal ID19132619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:42629160..42651585hg38UCSC Ensembl
Innerchr13:43203296..43225721hg19UCSC Ensembl
Innerchr13:42101296..42123721hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3822426
hg1922426
hg1822426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1635n100
Supporting Variantsnssv3523393
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)nsv1043400
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