A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250201



Internal ID21307774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153620648..153658366hg38UCSC Ensembl
Outerchr6:153616611..153659377hg38UCSC Ensembl
Innerchr6:153941783..153979501hg19UCSC Ensembl
Outerchr6:153937746..153980512hg19UCSC Ensembl
Innerchr6:153983476..154021194hg18UCSC Ensembl
Outerchr6:153979439..154022205hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3842767
hg1942767
hg1842767
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170284
Supporting Variants
SamplesNGO_37
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250201
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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