A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1656n100



Internal ID22787743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:54569291..54904412hg38UCSC Ensembl
chr13:55143426..55478547hg19UCSC Ensembl
chr13:54041427..54376548hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38335122
hg19335122
hg18335122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048599, nsv1051640
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1656n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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