A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018131



Internal ID19107348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77321320..77367209hg38UCSC Ensembl
Innerchr6:78031037..78076926hg19UCSC Ensembl
Innerchr6:78087756..78133645hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3845890
hg1945890
hg1845890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6023n100
Supporting Variantsnssv3659054
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)nsv1018131
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