A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061186



Internal ID19150405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17297113..17411092hg38UCSC Ensembl
Innerchr17:17200427..17314406hg19UCSC Ensembl
Innerchr17:17141152..17255131hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38113980
hg19113980
hg18113980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560427
Samples
Known GenesNT5M
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061186
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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