A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11729n54



Internal ID20145153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152319159..152373073hg38UCSC Ensembl
chr7:152016244..152070158hg19UCSC Ensembl
chr7:151647177..151701091hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3853915
hg1953915
hg1853915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609050, nsv609052
SamplesNINDS_7
Known GenesKMT2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11729n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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