A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515755



Internal ID15442812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161019278..161093126hg38UCSC Ensembl
Innerchr4:161940430..162014278hg19UCSC Ensembl
Innerchr4:162159880..162233728hg18UCSC Ensembl
Innerchr4:162298035..162371883hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3873849
hg1973849
hg1873849
hg1773849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662691, nssv655974, nssv680619, nssv688362, nssv667860, nssv671109, nssv673929, nssv657190, nssv683030, nssv670807, nssv664691, nssv682113, nssv660759, nssv659925, nssv688582, nssv683132, nssv665783, nssv689467, nssv691234, nssv674643, nssv669693, nssv686722, nssv685619
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515755
Frequency
Sample Size2026
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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