A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999318



Internal ID19158854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99205206..99230565hg38UCSC Ensembl
Innerchr3:98924050..98949409hg19UCSC Ensembl
Innerchr3:100406740..100432099hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3825360
hg1925360
hg1825360
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4825n100
Supporting Variantsnssv3603392, nssv3603391, nssv3603393, nssv3603396, nssv3603397, nssv3603390, nssv3603394, nssv3603395
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)nsv999318
Frequency
Sample Size11257
Observed Gain5
Observed Loss3
Observed Complex0
Frequencyn/a


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