A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718876



Internal ID18670471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10040025..10133251hg38UCSC Ensembl
Innerchr16:10133882..10227108hg19UCSC Ensembl
Innerchr16:10041383..10134609hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3893227
hg1993227
hg1893227
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043654
Supporting Variants
Samples
Known GenesGRIN2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718876
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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