A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011364



Internal ID19100581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128665668..128705613hg38UCSC Ensembl
Innerchr3:128384511..128424456hg19UCSC Ensembl
Innerchr3:129867201..129907146hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3839946
hg1939946
hg1839946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4857n100
Supporting Variantsnssv3603527, nssv3603529, nssv3603526, nssv3603528
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)nsv1011364
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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