A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061146



Internal ID18803677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46576019..46707604hg38UCSC Ensembl
Innerchr17:44653385..44784970hg19UCSC Ensembl
Innerchr17:42008701..42140153hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38131586
hg19131586
hg18131453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3260n100
Supporting Variantsnssv3568599
Samples
Known GenesARL17A, ARL17B, NSF, NSFP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061146
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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