A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067209



Internal ID19156428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22981863..23100328hg38UCSC Ensembl
Innerchr18:20561826..20680292hg19UCSC Ensembl
Innerchr18:18815824..18934290hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38118466
hg19118467
hg18118467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564133, nssv3564134
Samples
Known GenesRBBP8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067209
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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