A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718845



Internal ID18670440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6606773..6635321hg38UCSC Ensembl
Innerchr16:6656774..6685322hg19UCSC Ensembl
Innerchr16:6596775..6625323hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3828549
hg1928549
hg1828549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046705
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718845
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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