A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560942



Internal ID18859223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21425355..21601624hg38UCSC Ensembl
Innerchr17:21328667..21504890hg19UCSC Ensembl
Innerchr17:21269260..21445483hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38176270
hg19176224
hg18176224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064846
Supporting Variants
Samples
Known GenesC17orf51
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560942
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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