A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033905



Internal ID18776439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4955592..5080670hg38UCSC Ensembl
Innerchr6:4955826..5080904hg19UCSC Ensembl
Innerchr6:4900825..5025903hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38125079
hg19125079
hg18125079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747906
Samples
Known GenesRPP40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033905
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