A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648887



Internal ID18947168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82916908..82967362hg38UCSC Ensembl
Innerchr6:83626627..83677081hg19UCSC Ensembl
Innerchr6:83683346..83733800hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3850455
hg1950455
hg1850455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030196
Supporting Variants
Samples
Known GenesUBE3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648887
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