A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005997



Internal ID19095215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165548278..165592958hg38UCSC Ensembl
Innerchr3:165266066..165310746hg19UCSC Ensembl
Innerchr3:166748760..166793440hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3844681
hg1944681
hg1844681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4974n100
Supporting Variantsnssv3612648, nssv3612647
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)nsv1005997
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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