A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035255



Internal ID18777786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39044165..39141199hg38UCSC Ensembl
Innerchr13:39618302..39715336hg19UCSC Ensembl
Innerchr13:38516302..38613336hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3897035
hg1997035
hg1897035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523381
Samples
Known GenesNHLRC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035255
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