A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030634



Internal ID18773165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24938049..25039933hg38UCSC Ensembl
Innerchr6:24938277..25040161hg19UCSC Ensembl
Innerchr6:25046256..25148140hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38101885
hg19101885
hg18101885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654839
Samples
Known GenesFAM65B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030634
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