A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250321



Internal ID21310718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24950971..24964250hg38UCSC Ensembl
Outerchr6:24947577..24966461hg38UCSC Ensembl
Innerchr6:24951199..24964478hg19UCSC Ensembl
Outerchr6:24947805..24966689hg19UCSC Ensembl
Innerchr6:25059178..25072457hg18UCSC Ensembl
Outerchr6:25055784..25074668hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3818885
hg1918885
hg1818885
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170285
Supporting Variants
SamplesPML_1
Known GenesFAM65B
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250321
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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