A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066752



Internal ID19155971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57610960..57633489hg38UCSC Ensembl
Innerchr17:55688321..55710850hg19UCSC Ensembl
Innerchr17:53043320..53065849hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3822530
hg1922530
hg1822530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567704
Samples
Known GenesMSI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066752
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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