A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560082



Internal ID18511677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2586358..2635403hg38UCSC Ensembl
Innerchr17:2489652..2538697hg19UCSC Ensembl
Innerchr17:2436402..2485447hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3849046
hg1949046
hg1849046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055844
Supporting Variants
Samples
Known GenesPAFAH1B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560082
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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