A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7251n100



Internal ID22793338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84303435..84356419hg38UCSC Ensembl
chr8:85215670..85268654hg19UCSC Ensembl
chr8:85378225..85431209hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3852985
hg1952985
hg1852985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034144, nsv1028784
Samples
Known GenesRALYL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7251n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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