A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559347



Internal ID18510942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56629882..56684830hg38UCSC Ensembl
Innerchr16:56663794..56718742hg19UCSC Ensembl
Innerchr16:55221295..55276243hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3854949
hg1954949
hg1854949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067329
Supporting Variants
Samples
Known GenesMT1A, MT1B, MT1DP, MT1F, MT1G, MT1H, MT1IP, MT1JP, MT1M, MT1X
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559347
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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