A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066611



Internal ID18809142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46317034..46707604hg38UCSC Ensembl
Innerchr17:44394400..44784970hg19UCSC Ensembl
Innerchr17:41750175..42140153hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38390571
hg19390571
hg18389979
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3254n100
Supporting Variantsnssv3563374, nssv3563376, nssv3563375, nssv3563373
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)nsv1066611
Frequency
Sample Size29084
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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