A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054101



Internal ID19143320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22511531..22555272hg38UCSC Ensembl
Innerchr11:22533077..22576818hg19UCSC Ensembl
Innerchr11:22489653..22533394hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3843742
hg1943742
hg1843742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516508
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054101
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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