A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557134



Internal ID18508729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11342133..11449038hg38UCSC Ensembl
Innerchr16:11435990..11542894hg19UCSC Ensembl
Innerchr16:11343491..11450395hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38106906
hg19106905
hg18106905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048116
Supporting Variants
Samples
Known GenesRMI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557134
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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