A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560056



Internal ID18511651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:842299..977465hg38UCSC Ensembl
Innerchr17:745539..880705hg19UCSC Ensembl
Innerchr17:692289..827455hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38135167
hg19135167
hg18135167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058467
Supporting Variants
Samples
Known GenesNXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560056
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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