A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169543



Internal ID21313776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26392633..26397852hg38UCSC Ensembl
Outerchr3:26384700..26404482hg38UCSC Ensembl
Innerchr3:26434124..26439343hg19UCSC Ensembl
Outerchr3:26426191..26445973hg19UCSC Ensembl
Innerchr3:26409128..26414347hg18UCSC Ensembl
Outerchr3:26401195..26420977hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3819783
hg1919783
hg1819783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247657, nssv14250634
SamplesMLY_2, NGO_2
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169543
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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