A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010822



Internal ID18753354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..115870hg38UCSC Ensembl
Innerchr3:60333..157553hg19UCSC Ensembl
Innerchr3:35333..132553hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3897216
hg1997221
hg1897221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590200, nssv3590201, nssv3590199
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)nsv1010822
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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