A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11491n54



Internal ID20144915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88039690..88043355hg38UCSC Ensembl
chr7:87669005..87672670hg19UCSC Ensembl
chr7:87506941..87510606hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg383666
hg193666
hg183666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607736, nsv607735, nsv607737
Samples
Known GenesADAM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11491n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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