A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170215



Internal ID21314276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35827..80854hg38UCSC Ensembl
Outerchr16:12016..88517hg38UCSC Ensembl
Innerchr16:85827..130853hg19UCSC Ensembl
Outerchr16:62016..138516hg19UCSC Ensembl
Innerchr16:25827..70853hg18UCSC Ensembl
Outerchr16:2016..78516hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3876502
hg1976501
hg1876501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251041
SamplesSNI_5
Known GenesDDX11L10, LOC100288778, MIR6859-1, MIR6859-2, MPG, NPRL3, POLR3K, RHBDF1, SNRNP25
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170215
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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