A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061392



Internal ID19150611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54756503..54817463hg38UCSC Ensembl
Innerchr17:52833864..52894824hg19UCSC Ensembl
Innerchr17:50188863..50249823hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3860961
hg1960961
hg1860961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566106
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)nsv1061392
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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