A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5567n100



Internal ID22791654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9898850..9926563hg38UCSC Ensembl
chr5:9898962..9926675hg19UCSC Ensembl
chr5:9951962..9979675hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3827714
hg1927714
hg1827714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032580, nsv1017710, nsv1031285, nsv1019776, nsv1022404, nsv1028256, nsv1018405, nsv1024335, nsv1030621, nsv1034976, nsv1030798, nsv1034316, nsv1034130, nsv1027700, nsv1022268, nsv1027422
Samples
Known GenesLOC285692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5567n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss104
Observed Complex0
Frequencyn/a


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