A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657680



Internal ID18955961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65683455..65793538hg38UCSC Ensembl
Innerchr6:66393348..66503431hg19UCSC Ensembl
Innerchr6:66450069..66560152hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38110084
hg19110084
hg18110084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024973
Supporting Variants
Samples
Known GenesEYS, SLC25A51P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657680
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