A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv364n21



Internal ID20132085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178982284..178988936hg38UCSC Ensembl
chr5:178409285..178415937hg19UCSC Ensembl
chr5:178341891..178348543hg18UCSC Ensembl
chr5:178341891..178348543hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg386653
hg196653
hg186653
hg176653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516324, nsv527183
Samples
Known GenesGRM6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv364n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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