A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5557n54



Internal ID20138981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36190840..36195856hg38UCSC Ensembl
chr17:34606289..34611298hg19UCSC Ensembl
chr17:31630402..31635411hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg385017
hg195010
hg185010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574851, nsv574850, nsv574855
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5557n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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