A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035393



Internal ID18777924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15388065..15567957hg38UCSC Ensembl
Innerchr16:15481922..15661814hg19UCSC Ensembl
Innerchr16:15389423..15569315hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38179893
hg19179893
hg18179893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557963
Samples
Known GenesC16orf45, MPV17L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035393
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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