A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997858



Internal ID19157394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26498302..26560273hg38UCSC Ensembl
Innerchr3:26539793..26601764hg19UCSC Ensembl
Innerchr3:26514797..26576768hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3861972
hg1961972
hg1861972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4710n100
Supporting Variantsnssv3589554
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)nsv997858
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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