A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656586



Internal ID15393238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8725160..8726631hg38UCSC Ensembl
Innerchr18:8725158..8726629hg19UCSC Ensembl
Innerchr18:8715158..8716629hg18UCSC Ensembl
Innerchr18:8715158..8716629hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381472
hg191472
hg181472
hg171472
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517204
Supporting Variants
Samples
Known GenesSOGA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656586
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