A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057803



Internal ID18800334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18561260..19019420hg38UCSC Ensembl
Innerchr17:18464574..18922733hg19UCSC Ensembl
Innerchr17:18405299..18863458hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38458161
hg19458160
hg18458160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560533
Samples
Known GenesCCDC144B, FAM83G, FBXW10, FOXO3B, PRPSAP2, SLC5A10, TBC1D28, TRIM16L, TVP23B, ZNF286B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057803
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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