A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065759



Internal ID19154978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4405261..4476552hg38UCSC Ensembl
Innerchr17:4308556..4379847hg19UCSC Ensembl
Innerchr17:4255305..4326596hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3871292
hg1971292
hg1871292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560126, nssv3560127
Samples
Known GenesSPNS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065759
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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