A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047674



Internal ID19136893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3405372..3574519hg38UCSC Ensembl
Innerchr11:3426602..3595749hg19UCSC Ensembl
Innerchr11:3383178..3552325hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38169148
hg19169148
hg18169148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1018n100
Supporting Variantsnssv3518865
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)nsv1047674
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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