A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698448



Internal ID15088414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36187786..36199742hg38UCSC Ensembl
Innerchr18:33767749..33779705hg19UCSC Ensembl
Innerchr18:32021747..32033703hg18UCSC Ensembl
Innerchr18:32021747..32033703hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3811957
hg1911957
hg1811957
hg1711957
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522803
Supporting Variants
Samples
Known GenesMOCOS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698448
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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