A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011995



Internal ID19101213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99181961..99230565hg38UCSC Ensembl
Innerchr3:98900805..98949409hg19UCSC Ensembl
Innerchr3:100383495..100432099hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3848605
hg1948605
hg1848605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4822n100
Supporting Variantsnssv3603381, nssv3603376, nssv3603370, nssv3735186, nssv3603380, nssv3603379, nssv3603374, nssv3603371, nssv3603378, nssv3603372, nssv3603384, nssv3603369, nssv3603373, nssv3603386, nssv3603377, nssv3603375, nssv3603383, nssv3603382, nssv3603385
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)nsv1011995
Frequency
Sample Size11257
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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