A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516207



Internal ID15443500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:124920737..124924963hg38UCSC Ensembl
Innerchr4:125841892..125846118hg19UCSC Ensembl
Innerchr4:126061342..126065568hg18UCSC Ensembl
Innerchr4:126199497..126203723hg17UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg384227
hg194227
hg184227
hg174227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662932, nssv652630, nssv694885
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516207
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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