A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv95n21



Internal ID6314605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52864775..52882850hg19UCSC Ensembl
chr12:51151042..51169117hg18UCSC Ensembl
chr12:51151042..51169117hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv524862, nsv527439
Samples
Known GenesKRT6A, KRT6C
Method
Analysis
Platform
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)dgv95n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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