A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048187



Internal ID19137406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130574295..130609326hg38UCSC Ensembl
Innerchr9:133449682..133484713hg19UCSC Ensembl
Innerchr9:132439503..132474534hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3835032
hg1935032
hg1835032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7719n100
Supporting Variantsnssv3695256, nssv3695257
Samples
Known GenesFUBP3, LOC100272217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048187
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer