A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10873n54



Internal ID22778768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101855205..101907992hg38UCSC Ensembl
chr6:102303080..102355867hg19UCSC Ensembl
chr6:102409773..102462560hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3852788
hg1952788
hg1852788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604319, nsv604318, nsv604320
Samples1780862432_A
Known GenesGRIK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10873n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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