A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055622



Internal ID19144841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42460509..42477790hg38UCSC Ensembl
Innerchr18:40040474..40057755hg19UCSC Ensembl
Innerchr18:38294472..38311753hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3817282
hg1917282
hg1817282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3344n100
Supporting Variantsnssv3725324, nssv3725325
Samples
Known GenesLINC00907
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055622
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