A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998169



Internal ID19157706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68670067..68698250hg38UCSC Ensembl
Innerchr3:68719218..68747401hg19UCSC Ensembl
Innerchr3:68801908..68830091hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3828184
hg1928184
hg1828184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4772n100
Supporting Variantsnssv3594010, nssv3594011, nssv3594014, nssv3594012, nssv3594013
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)nsv998169
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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