A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11652n54



Internal ID20145076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142625892..142809818hg38UCSC Ensembl
chr7:142333406..142507502hg19UCSC Ensembl
chr7:142014398..142217629hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38183927
hg19174097
hg18203232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608629, nsv608631, nsv608628, nsv608626, nsv608627
SamplesHGDP00770, HGDP01311, HGDP01287, HGDP00542, HGDP00972
Known GenesMTRNR2L6, PRSS1, PRSS2, PRSS3P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11652n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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