A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048675



Internal ID18791206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8708895..8734684hg38UCSC Ensembl
Innerchr16:8802752..8828541hg19UCSC Ensembl
Innerchr16:8710253..8736042hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3825790
hg1925790
hg1825790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557107
Samples
Known GenesABAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048675
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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