A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025307



Internal ID19114525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86644777..86930482hg38UCSC Ensembl
Innerchr6:87354495..87640200hg19UCSC Ensembl
Innerchr6:87411214..87696919hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38285706
hg19285706
hg18285706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3750121
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)nsv1025307
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