A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055572



Internal ID19144791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22656779..22720816hg38UCSC Ensembl
Innerchr16:22668100..22732137hg19UCSC Ensembl
Innerchr16:22575601..22639638hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3864038
hg1964038
hg1864038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549109, nssv3549110
Samples
Known GenesMIR548AA2, MIR548D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055572
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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