A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064385



Internal ID18806916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36840494..36959363hg38UCSC Ensembl
Innerchr18:34420457..34539326hg19UCSC Ensembl
Innerchr18:32674455..32793324hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38118870
hg19118870
hg18118870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3334n100
Supporting Variantsnssv3725315
Samples
Known GenesKIAA1328
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064385
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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