A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056738



Internal ID18799269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:67021320..67091992hg38UCSC Ensembl
Innerchr16:67055223..67125895hg19UCSC Ensembl
Innerchr16:65612724..65683396hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3870673
hg1970673
hg1870673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559441
Samples
Known GenesCBFB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056738
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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