A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031923



Internal ID19121145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77626179..77649143hg38UCSC Ensembl
Innerchr6:78335896..78358860hg19UCSC Ensembl
Innerchr6:78392615..78415579hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3822965
hg1922965
hg1822965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747160
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)nsv1031923
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