A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988332



Internal ID12982282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4142954..4254904hg38UCSC Ensembl
Innerchr11:4164184..4276134hg19UCSC Ensembl
Innerchr11:4120760..4232710hg18UCSC Ensembl
Innerchr11:4120760..4232710hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38111951
hg19111951
hg18111951
hg17111951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34983
Supporting Variants
SamplesNA19144
Known GenesLOC100506082
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988332
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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