A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10783n54



Internal ID22778678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74122808..74142792hg38UCSC Ensembl
chr6:74832524..74852508hg19UCSC Ensembl
chr6:74889244..74909228hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3819985
hg1919985
hg1819985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603752, nsv603753
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10783n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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