A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037001



Internal ID18779532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9914166..10382625hg38UCSC Ensembl
Innerchr16:10008023..10476482hg19UCSC Ensembl
Innerchr16:9915524..10383983hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38468460
hg19468460
hg18468460
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2727n100
Supporting Variantsnssv3718873
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)nsv1037001
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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