A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037325



Internal ID18779856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8615311..8688379hg38UCSC Ensembl
Innerchr16:8709168..8782236hg19UCSC Ensembl
Innerchr16:8616669..8689737hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3873069
hg1973069
hg1873069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557105
Samples
Known GenesABAT, METTL22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037325
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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