A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062464



Internal ID18804995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46234092..46563264hg38UCSC Ensembl
Innerchr17:44311458..44640630hg19UCSC Ensembl
Innerchr17:41667235..41995946hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38329173
hg19329173
hg18328712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3241n100
Supporting Variantsnssv3550221
Samples
Known GenesARL17A, ARL17B, LOC644172, 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)nsv1062464
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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