A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv95n21



Internal ID11600773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52470991..52489066hg38UCSC Ensembl
chr12:52864775..52882850hg19UCSC Ensembl
chr12:51151042..51169117hg18UCSC Ensembl
chr12:51151042..51169117hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3818076
hg1918076
hg1818076
hg1718076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524862, nsv527439
Samples
Known GenesKRT6A, KRT6C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
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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