A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058951



Internal ID18801482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85702767..85768455hg38UCSC Ensembl
Innerchr16:85736373..85802061hg19UCSC Ensembl
Innerchr16:84293874..84359562hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3865689
hg1965689
hg1865689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3060n100
Supporting Variantsnssv3559968
Samples
Known GenesC16orf74, MIR1910, MIR7851
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058951
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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