A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11274n54



Internal ID20144698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38233704..38322024hg38UCSC Ensembl
chr7:38273305..38361625hg19UCSC Ensembl
chr7:38239830..38328150hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3888321
hg1988321
hg1888321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606630, nsv606625
SamplesNINDS_119
Known GenesTARP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11274n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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