A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516283



Internal ID15443576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62551843..63244640hg38UCSC Ensembl
Innerchr7:62012221..62705018hg19UCSC Ensembl
Innerchr7:61649656..62342453hg18UCSC Ensembl
Innerchr7:61456371..62149168hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38692798
hg19692798
hg18692798
hg17692798
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657031, nssv692105, nssv702213, nssv672879, nssv668236, nssv672500, nssv700300, nssv667780, nssv660660, nssv701039, nssv683935, nssv675977, nssv681562, nssv680590, nssv704745, nssv686997, nssv669141, nssv662440, nssv657880, nssv656484, nssv678832, nssv656178, nssv655292, nssv692013, nssv705472, nssv704130, nssv677631, nssv700468, nssv667330
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516283
Frequency
Sample Size2026
Observed Gain9
Observed Loss20
Observed Complex0
Frequencyn/a


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