A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037707



Internal ID18780238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9984933..10436036hg38UCSC Ensembl
Innerchr16:10078790..10529893hg19UCSC Ensembl
Innerchr16:9986291..10437394hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38451104
hg19451104
hg18451104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2727n100
Supporting Variantsnssv3557122
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)nsv1037707
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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