A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv390n21



Internal ID22766582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99523553..99524733hg38UCSC Ensembl
chr6:99971429..99972609hg19UCSC Ensembl
chr6:100078150..100079330hg18UCSC Ensembl
chr6:100078150..100079330hg17UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381181
hg191181
hg181181
hg171181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv517990, nsv528990
Samples
Known GenesTSTD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv390n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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