A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6077n54



Internal ID22773972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76692089..76763414hg38UCSC Ensembl
chr18:74404045..74475370hg19UCSC Ensembl
chr18:72533033..72604358hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3871326
hg1971326
hg1871326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577694, nsv577691, nsv577689, nsv577688, nsv577692, nsv577693
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6077n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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