A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055897



Internal ID19145116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:5709321..5731723hg38UCSC Ensembl
Innerchr17:5612641..5635043hg19UCSC Ensembl
Innerchr17:5553365..5575767hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3822403
hg1922403
hg1822403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560135
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055897
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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