A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054751



Internal ID18797282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:17327118..17359994hg38UCSC Ensembl
Innerchr16:17420975..17453851hg19UCSC Ensembl
Innerchr16:17328476..17361352hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3832877
hg1932877
hg1832877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3558096
Samples
Known GenesXYLT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054751
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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