A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052626



Internal ID18795157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125642543..125837198hg38UCSC Ensembl
Innerchr9:128404822..128599477hg19UCSC Ensembl
Innerchr9:127444643..127639298hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38194656
hg19194656
hg18194656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695230
Samples
Known GenesMAPKAP1, PBX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052626
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