A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066256



Internal ID19155475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54756503..54784544hg38UCSC Ensembl
Innerchr17:52833864..52861905hg19UCSC Ensembl
Innerchr17:50188863..50216904hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3828042
hg1928042
hg1828042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566105
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)nsv1066256
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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