A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055295



Internal ID18797826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29005207..29114752hg38UCSC Ensembl
Innerchr16:29016528..29126073hg19UCSC Ensembl
Innerchr16:28924029..29033574hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38109546
hg19109546
hg18109546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549148
Samples
Known GenesRRN3P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055295
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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