A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057064



Internal ID18799595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46284631..46576019hg38UCSC Ensembl
Innerchr17:44361997..44653385hg19UCSC Ensembl
Innerchr17:41717774..42008701hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38291389
hg19291389
hg18290928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3248n100
Supporting Variantsnssv3565786
Samples
Known GenesARL17A, ARL17B, LRRC37A, LRRC37A2, NSFP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057064
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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