A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv150n21



Internal ID22766342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57658436..57661366hg38UCSC Ensembl
chr15:57950634..57953564hg19UCSC Ensembl
chr15:55737926..55740856hg18UCSC Ensembl
chr15:55737926..55740856hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382931
hg192931
hg182931
hg172931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524912, nsv518825
Samples
Known GenesGCOM1, MYZAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv150n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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