A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557123



Internal ID18508718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9998145..10427239hg38UCSC Ensembl
Innerchr16:10092002..10521096hg19UCSC Ensembl
Innerchr16:9999503..10428597hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38429095
hg19429095
hg18429095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042727
Supporting Variants
Samples
Known GenesATF7IP2, GRIN2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557123
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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