A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056758



Internal ID18799289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84761857..84886461hg38UCSC Ensembl
Innerchr16:84795463..84920067hg19UCSC Ensembl
Innerchr16:83352964..83477568hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38124605
hg19124605
hg18124605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559962
Samples
Known GenesCRISPLD2, USP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056758
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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