A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648877



Internal ID18947158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82010915..82027739hg38UCSC Ensembl
Innerchr6:82720632..82737456hg19UCSC Ensembl
Innerchr6:82777351..82794175hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3816825
hg1916825
hg1816825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021793
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)nssv3648877
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