A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169922



Internal ID21313733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42231350..42268927hg38UCSC Ensembl
Outerchr6:42226497..42270556hg38UCSC Ensembl
Innerchr6:42199088..42236665hg19UCSC Ensembl
Outerchr6:42194235..42238294hg19UCSC Ensembl
Innerchr6:42307066..42344643hg18UCSC Ensembl
Outerchr6:42302213..42346272hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3844060
hg1944060
hg1844060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244070
SamplesNGO_23
Known GenesTRERF1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169922
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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