A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11716n54



Internal ID22779611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149759270..149787971hg38UCSC Ensembl
chr7:149456359..149485059hg19UCSC Ensembl
chr7:149087292..149115992hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3828702
hg1928701
hg1828701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608985, nsv608986
Samples1782681313_A, HGDP01163
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11716n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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