A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5710n100



Internal ID22791797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84477630..84620325hg38UCSC Ensembl
chr5:83773448..83916143hg19UCSC Ensembl
chr5:83809204..83951899hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38142696
hg19142696
hg18142696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018066, nsv1028544, nsv1027978, nsv1030247, nsv1030573
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)dgv5710n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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