A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169728



Internal ID21313539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86604868..86615738hg38UCSC Ensembl
Outerchr7:86600286..86622960hg38UCSC Ensembl
Innerchr7:86234184..86245054hg19UCSC Ensembl
Outerchr7:86229602..86252276hg19UCSC Ensembl
Innerchr7:86072120..86082990hg18UCSC Ensembl
Outerchr7:86067538..86090212hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3822675
hg1922675
hg1822675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249517
SamplesMLY_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169728
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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