A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985433



Internal ID12982285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4144687..4304562hg38UCSC Ensembl
Innerchr11:4165917..4325792hg19UCSC Ensembl
Innerchr11:4122493..4282368hg18UCSC Ensembl
Innerchr11:4122493..4282368hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38159876
hg19159876
hg18159876
hg17159876
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985433
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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