A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556938



Internal ID18508533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10765..207261hg38UCSC Ensembl
Innerchr16:60765..257260hg19UCSC Ensembl
Innerchr16:765..197261hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38196497
hg19196496
hg18196497
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050276
Supporting Variants
Samples
Known GenesDDX11L10, HBA1, HBA2, HBM, HBQ1, HBZ, LOC100288778, LUC7L, MIR6859-1, MIR6859-2, MPG, NPRL3, POLR3K, RHBDF1, SNRNP25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556938
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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