A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044849



Internal ID19134068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28709718..28763772hg38UCSC Ensembl
Innerchr11:28731265..28785319hg19UCSC Ensembl
Innerchr11:28687841..28741895hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3854055
hg1954055
hg1854055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511360
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)nsv1044849
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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