A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064223



Internal ID18806754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23740325..23784214hg38UCSC Ensembl
Innerchr16:23751646..23795535hg19UCSC Ensembl
Innerchr16:23659147..23703036hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3843890
hg1943890
hg1843890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549126
Samples
Known GenesCHP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064223
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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