A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170027



Internal ID21314088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:97574837..97696261hg38UCSC Ensembl
Outerchr6:97573465..97703518hg38UCSC Ensembl
Innerchr6:98022713..98144137hg19UCSC Ensembl
Outerchr6:98021341..98151394hg19UCSC Ensembl
Innerchr6:98129434..98250858hg18UCSC Ensembl
Outerchr6:98128062..98258115hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38130054
hg19130054
hg18130054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247644
SamplesNGO_22
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170027
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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