A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053090



Internal ID18795621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5304641..5327595hg38UCSC Ensembl
Innerchr16:5354642..5377596hg19UCSC Ensembl
Innerchr16:5294643..5317597hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3822955
hg1922955
hg1822955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2698n100
Supporting Variantsnssv3556995, nssv3556996
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053090
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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