A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169737



Internal ID21313548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39101136..39104258hg38UCSC Ensembl
Outerchr6:39099091..39115512hg38UCSC Ensembl
Innerchr6:39068912..39072034hg19UCSC Ensembl
Outerchr6:39066867..39083288hg19UCSC Ensembl
Innerchr6:39176890..39180012hg18UCSC Ensembl
Outerchr6:39174845..39191266hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3816422
hg1916422
hg1816422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241632
SamplesNGO_39
Known GenesSAYSD1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169737
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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