A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561009



Internal ID18859290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22167253..22720229hg38UCSC Ensembl
Innerchr17:21693859..22219556hg19UCSC Ensembl
Innerchr17:21617989..22143683hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg38552977
hg19525698
hg18525695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064900
Supporting Variants
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561009
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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