A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11137n54



Internal ID22779032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1665198..1669751hg38UCSC Ensembl
chr7:1704834..1709387hg19UCSC Ensembl
chr7:1671360..1675913hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg384554
hg194554
hg184554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605831, nsv605830, nsv605829, nsv605828
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11137n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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