A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063419



Internal ID18805950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46088437..46576019hg38UCSC Ensembl
Innerchr17:44165803..44653385hg19UCSC Ensembl
Innerchr17:41521621..42008701hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38487583
hg19487583
hg18487081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3188n100
Supporting Variantsnssv3548377, nssv3548375, nssv3548376
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, 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)nsv1063419
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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