A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3658823



Internal ID18957104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76288541..76307348hg38UCSC Ensembl
Innerchr6:76998258..77017065hg19UCSC Ensembl
Innerchr6:77054978..77073785hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3818808
hg1918808
hg1818808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028432
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)nssv3658823
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