A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517324



Internal ID15444617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15094899..15104412hg38UCSC Ensembl
Innerchr4:15096523..15106036hg19UCSC Ensembl
Innerchr4:14705621..14715134hg18UCSC Ensembl
Innerchr4:14772792..14782305hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg389514
hg199514
hg189514
hg179514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681669, nssv667128, nssv685823, nssv686882, nssv651722, nssv656519, nssv695781, nssv668019, nssv687729, nssv687619, nssv672744, nssv680308, nssv678870, nssv689315
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517324
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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