A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11284n54



Internal ID22779179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39505188..39510237hg38UCSC Ensembl
chr7:39544787..39549836hg19UCSC Ensembl
chr7:39511312..39516361hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385050
hg195050
hg185050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606677, nsv606678
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11284n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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