A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062128



Internal ID18804659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46323689..46645464hg38UCSC Ensembl
Innerchr17:44401055..44722830hg19UCSC Ensembl
Innerchr17:41756820..42078146hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38321776
hg19321776
hg18321327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3253n100
Supporting Variantsnssv3563428, nssv3563429, nssv3563425, nssv3563430, nssv3723640, nssv3723641, nssv3563427, nssv3563426, nssv3563424
Samples
Known GenesARL17A, ARL17B, LRRC37A, LRRC37A2, 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)nsv1062128
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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