A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv90n21



Internal ID22766282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14268178..14275184hg38UCSC Ensembl
chr12:14421112..14428118hg19UCSC Ensembl
chr12:14312379..14319385hg18UCSC Ensembl
chr12:14312379..14319385hg17UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg387007
hg197007
hg187007
hg177007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516257, nsv526448
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv90n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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