A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027814



Internal ID18770345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18104576..18155276hg38UCSC Ensembl
Innerchr7:18144199..18194899hg19UCSC Ensembl
Innerchr7:18110724..18161424hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3850701
hg1950701
hg1850701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752919
Samples
Known GenesHDAC9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027814
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer