A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11714n54



Internal ID20145138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149748496..149787971hg38UCSC Ensembl
chr7:149445585..149485059hg19UCSC Ensembl
chr7:149076518..149115992hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3839476
hg1939475
hg1839475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608982, nsv608983, nsv608980
Samples
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11714n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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