A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557124



Internal ID18508719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10016183..10034307hg38UCSC Ensembl
Innerchr16:10110040..10128164hg19UCSC Ensembl
Innerchr16:10017541..10035665hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3818125
hg1918125
hg1818125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050835
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)nssv3557124
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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