A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057935



Internal ID19147154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:51366466..51428797hg38UCSC Ensembl
Innerchr18:48892836..48955167hg19UCSC Ensembl
Innerchr18:47146834..47209165hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3862332
hg1962332
hg1862332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3357n100
Supporting Variantsnssv3726077
Samples
Known GenesLOC100287225
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057935
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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