A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062584



Internal ID18805115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46211152..46707300hg38UCSC Ensembl
Innerchr17:44288518..44784666hg19UCSC Ensembl
Innerchr17:41644295..42139849hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38496149
hg19496149
hg18495555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3198n100
Supporting Variantsnssv3557524
Samples
Known GenesARL17A, ARL17B, KANSL1, LOC644172, 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)nsv1062584
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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