A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561018



Internal ID18859299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22319095..22709212hg38UCSC Ensembl
Innerchr17:21845701..22208539hg19UCSC Ensembl
Innerchr17:21769828..22132666hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg38390118
hg19362839
hg18362839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066648
Supporting Variants
Samples
Known GenesFLJ36000, MTRNR2L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561018
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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