A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv25e196



Internal ID22757695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97553627..97679750hg38UCSC Ensembl
chr5:96889331..97015454hg19UCSC Ensembl
chr5:96915087..97041210hg18UCSC Ensembl
chr5:96915087..97041210hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38126124
hg19126124
hg18126124
hg17126124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2422224, esv2422198, esv2422222
SamplesND01703, ND04275, ND04103
Known GenesLOC102546227
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)dgv25e196
Frequency
Sample Size181
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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