A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046864



Internal ID19136083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6911165..6935272hg38UCSC Ensembl
Innerchr11:6932396..6956503hg19UCSC Ensembl
Innerchr11:6888972..6913079hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824108
hg1924108
hg1824108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708508
Samples
Known GenesOR2D3, ZNF215
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046864
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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