A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5811n100



Internal ID22791898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135705961..135730733hg38UCSC Ensembl
chr5:135041650..135066422hg19UCSC Ensembl
chr5:135069549..135094321hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3824773
hg1924773
hg1824773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018805, nsv1017948
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)dgv5811n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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