A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5395n54



Internal ID22773290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:948888..949861hg38UCSC Ensembl
chr17:852128..853101hg19UCSC Ensembl
chr17:798878..799851hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574115, nsv574109, nsv574105, nsv574108, nsv574107, nsv574106
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5395n54
Frequency
Sample Size17421
Observed Gain136
Observed Loss44
Observed Complex0
Frequencyn/a


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