A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026597



Internal ID19115815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13634437..13689650hg38UCSC Ensembl
Innerchr6:13634669..13689882hg19UCSC Ensembl
Innerchr6:13742648..13797861hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3855214
hg1955214
hg1855214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654791
Samples
Known GenesRANBP9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026597
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