A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506214



Internal ID18804495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76956116..77017224hg38UCSC Ensembl
Innerchr11:76667160..76728268hg19UCSC Ensembl
Innerchr11:76344808..76405916hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3861109
hg1961109
hg1861109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040833
Supporting Variants
Samples
Known GenesACER3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506214
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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