A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022052



Internal ID18764586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33121909..33278846hg38UCSC Ensembl
Innerchr9:33121907..33278844hg19UCSC Ensembl
Innerchr9:33111907..33268844hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38156938
hg19156938
hg18156938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7516n100
Supporting Variantsnssv3688870
Samples
Known GenesB4GALT1, BAG1, CHMP5, LOC101929639, SPINK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022052
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