A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520144



Internal ID18471739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105642307..105724996hg38UCSC Ensembl
Innerchr11:105513034..105595722hg19UCSC Ensembl
Innerchr11:105018244..105100932hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3882690
hg1982689
hg1882689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053687
Supporting Variants
Samples
Known GenesGRIA4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520144
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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