A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718874



Internal ID18670469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9931545..10024135hg38UCSC Ensembl
Innerchr16:10025402..10117992hg19UCSC Ensembl
Innerchr16:9932903..10025493hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3892591
hg1992591
hg1892591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045882
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)nssv3718874
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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