A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061271



Internal ID18803802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84707543..84729856hg38UCSC Ensembl
Innerchr16:84741149..84763462hg19UCSC Ensembl
Innerchr16:83298650..83320963hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3822314
hg1922314
hg1822314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559960
Samples
Known GenesUSP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061271
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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