A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015549



Internal ID19104766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5593732..5630235hg38UCSC Ensembl
Innerchr6:5593965..5630468hg19UCSC Ensembl
Innerchr6:5538964..5575467hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3836504
hg1936504
hg1836504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654742
Samples
Known GenesFARS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015549
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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