A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247548



Internal ID21303591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163215141..163223938hg38UCSC Ensembl
Outerchr6:163214833..163224768hg38UCSC Ensembl
Innerchr6:163636173..163644970hg19UCSC Ensembl
Outerchr6:163635865..163645800hg19UCSC Ensembl
Innerchr6:163556163..163564960hg18UCSC Ensembl
Outerchr6:163555855..163565790hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg389936
hg199936
hg189936
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169993
Supporting Variants
SamplesMLY_7
Known GenesPACRG
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247548
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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