A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5717n100



Internal ID22791804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93877558..93943511hg38UCSC Ensembl
chr5:93213264..93279216hg19UCSC Ensembl
chr5:93239020..93304972hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3865954
hg1965953
hg1865953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028893, nsv1020849
Samples
Known GenesFAM172A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5717n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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