A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010759



Internal ID19099976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99174666..99230565hg38UCSC Ensembl
Innerchr3:98893510..98949409hg19UCSC Ensembl
Innerchr3:100376200..100432099hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3855900
hg1955900
hg1855900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4822n100
Supporting Variantsnssv3603337, nssv3603338, nssv3603356, nssv3603355, nssv3603342, nssv3603353, nssv3603345, nssv3603359, nssv3603346, nssv3603336, nssv3603347, nssv3603341, nssv3603348, nssv3603360, nssv3603344, nssv3603349, nssv3603362, nssv3603354, nssv3603358, nssv3603350, nssv3603357, nssv3603343, nssv3603340, nssv3603339, nssv3603352, nssv3603361, nssv3603351
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)nsv1010759
Frequency
Sample Size11257
Observed Gain27
Observed Loss0
Observed Complex0
Frequencyn/a


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