A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978881



Internal ID12979293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81742510..82049110hg38UCSC Ensembl
Innerchr11:81453552..81760152hg19UCSC Ensembl
Innerchr11:81131200..81437800hg18UCSC Ensembl
Innerchr11:81131200..81437800hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38306601
hg19306601
hg18306601
hg17306601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34646
Supporting Variants
SamplesNA12753
Known GenesMIR4300
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978881
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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