A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11184n54



Internal ID22779079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8644051..8798213hg38UCSC Ensembl
chr7:8683681..8837843hg19UCSC Ensembl
chr7:8650206..8804368hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38154163
hg19154163
hg18154163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606091, nsv606090
Samples
Known GenesNXPH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11184n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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