A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060558



Internal ID19149777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56081671..56096102hg38UCSC Ensembl
Innerchr17:54159032..54173463hg19UCSC Ensembl
Innerchr17:51514031..51528462hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3814432
hg1914432
hg1814432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3267n100
Supporting Variantsnssv3566133, nssv3724985
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)nsv1060558
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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