A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11712n54



Internal ID20145136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149188785..149250188hg38UCSC Ensembl
chr7:148885877..148947279hg19UCSC Ensembl
chr7:148516810..148578212hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3861404
hg1961403
hg1861403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608975, nsv608974
Samples1780862101_A
Known GenesZNF212, ZNF282
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11712n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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