A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029816



Internal ID19119035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153676272..153712427hg38UCSC Ensembl
Innerchr6:153997407..154033562hg19UCSC Ensembl
Innerchr6:154039100..154075255hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3836156
hg1936156
hg1836156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654479
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)nsv1029816
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