A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169975



Internal ID21314036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110074988..110094225hg38UCSC Ensembl
Outerchr6:110073703..110095665hg38UCSC Ensembl
Innerchr6:110396191..110415428hg19UCSC Ensembl
Outerchr6:110394906..110416868hg19UCSC Ensembl
Innerchr6:110502884..110522121hg18UCSC Ensembl
Outerchr6:110501599..110523561hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3821963
hg1921963
hg1821963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251576
SamplesMLY_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169975
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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