A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043863



Internal ID19133082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3405372..3597187hg38UCSC Ensembl
Innerchr11:3426602..3618417hg19UCSC Ensembl
Innerchr11:3383178..3574993hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38191816
hg19191816
hg18191816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1018n100
Supporting Variantsnssv3507412
Samples
Known GenesLOC650368
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043863
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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