A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516664



Internal ID15097271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21638256..22743028hg38UCSC Ensembl
Innerchr17:21539613..22242355hg19UCSC Ensembl
Innerchr17:21480206..22166482hg18UCSC Ensembl
Innerchr17:21480206..22166482hg17UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381104773
hg19702743
hg18686277
hg17686277
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670000, nssv678457, nssv694904
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516664
Frequency
Sample Size2026
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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