A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998978



Internal ID19158514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152625026..152638401hg38UCSC Ensembl
Innerchr3:152342815..152356190hg19UCSC Ensembl
Innerchr3:153825505..153838880hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3813376
hg1913376
hg1813376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4923n100
Supporting Variantsnssv3741541
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998978
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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