A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007329



Internal ID19096548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44964987..45004163hg38UCSC Ensembl
Innerchr4:44967004..45006180hg19UCSC Ensembl
Innerchr4:44661761..44700937hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3839177
hg1939177
hg1839177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5199n100
Supporting Variantsnssv3739378, nssv3739376, nssv3625097, nssv3625102, nssv3625100, nssv3739380, nssv3625096, nssv3739381, nssv3625098, nssv3739377, nssv3739383, nssv3625103, nssv3625101, nssv3739382, nssv3739379, nssv3625099
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)nsv1007329
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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