A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3173n100



Internal ID22789260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41354648..41371345hg38UCSC Ensembl
chr17:39510900..39527597hg19UCSC Ensembl
chr17:36764426..36781123hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3816698
hg1916698
hg1816698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060030, nsv1055193, nsv1065153, nsv1061505, nsv1059490, nsv1060668
Samples
Known GenesKRT33B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3173n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer