A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031204



Internal ID19120425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120526567..120549392hg38UCSC Ensembl
Innerchr6:120847713..120870538hg19UCSC Ensembl
Innerchr6:120889412..120912237hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3822826
hg1922826
hg1822826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654339
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)nsv1031204
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