A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11490n54



Internal ID20144914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88039690..88042271hg38UCSC Ensembl
chr7:87669005..87671586hg19UCSC Ensembl
chr7:87506941..87509522hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382582
hg192582
hg182582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607732, nsv607734, nsv607738, nsv607733
Samples
Known GenesADAM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11490n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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