A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007017



Internal ID19096235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21217514..21302104hg38UCSC Ensembl
Innerchr3:21259006..21343596hg19UCSC Ensembl
Innerchr3:21234010..21318600hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3884591
hg1984591
hg1884591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4690n100
Supporting Variantsnssv3593132, nssv3593134, nssv3593133, nssv3593130, nssv3593131
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)nsv1007017
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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