A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065653



Internal ID18808184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:80187297..80257174hg38UCSC Ensembl
Innerchr18:77945180..78015057hg19UCSC Ensembl
Innerchr18:76046171..76116029hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3869878
hg1969878
hg1869859
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723250, nssv3563105
Samples
Known GenesPARD6G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065653
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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