A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5834n100



Internal ID22791921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176033072..176204967hg38UCSC Ensembl
chr5:175460075..175631970hg19UCSC Ensembl
chr5:175392681..175564576hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38171896
hg19171896
hg18171896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017314, nsv1015176, nsv1027493, nsv1034805, nsv1032438, nsv1020450, nsv1025451
Samples
Known GenesFAM153B, LOC100507387, LOC100996385, LOC643201
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5834n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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