A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11721n54



Internal ID20145145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150901404..150970122hg38UCSC Ensembl
chr7:150598492..150667210hg19UCSC Ensembl
chr7:150229425..150298143hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3868719
hg1968719
hg1868719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609001, nsv609000
SamplesHGDP01027
Known GenesKCNH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11721n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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