A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060255



Internal ID18802786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46127008..46323689hg38UCSC Ensembl
Innerchr17:44204374..44401055hg19UCSC Ensembl
Innerchr17:41560151..41756820hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38196682
hg19196682
hg18196670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3206n100
Supporting Variantsnssv3720897, nssv3720898
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060255
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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