A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648859



Internal ID18947140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80599496..80664982hg38UCSC Ensembl
Innerchr6:81309213..81374699hg19UCSC Ensembl
Innerchr6:81365932..81431418hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3865487
hg1965487
hg1865487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015520
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648859
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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