A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11291n54



Internal ID22779186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40332994..40388803hg38UCSC Ensembl
chr7:40372593..40428402hg19UCSC Ensembl
chr7:40339118..40394927hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3855810
hg1955810
hg1855810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606713, nsv606712
Samples
Known GenesC7orf10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11291n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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