A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5737n100



Internal ID22791824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100290153..100513939hg38UCSC Ensembl
chr5:99625857..99849643hg19UCSC Ensembl
chr5:99653756..99877542hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38223787
hg19223787
hg18223787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019588, nsv1026636
Samples
Known GenesLOC100133050
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5737n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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