A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv376n21



Internal ID20132097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29577048..29582841hg38UCSC Ensembl
chr6:29544825..29550618hg19UCSC Ensembl
chr6:29652804..29658597hg18UCSC Ensembl
chr6:29652804..29658597hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg385794
hg195794
hg185794
hg175794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527592, nsv522325
Samples
Known GenesSNORD32B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv376n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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