A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515566



Internal ID15443177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35337799..35441180hg38UCSC Ensembl
Innerchr17:33664818..33768199hg19UCSC Ensembl
Innerchr17:30688931..30792312hg18UCSC Ensembl
Innerchr17:30688931..30792312hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38103382
hg19103382
hg18103382
hg17103382
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679424, nssv685161, nssv655753, nssv663544, nssv690238, nssv663924, nssv705635, nssv682841, nssv686085, nssv691329, nssv687242, nssv681737, nssv667652
Samples
Known GenesSLFN11, SLFN12, SLFN13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515566
Frequency
Sample Size2026
Observed Gain1
Observed Loss12
Observed Complex0
Frequencyn/a


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