A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055525



Internal ID19144744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357088..35441180hg38UCSC Ensembl
Innerchr17:33684107..33768199hg19UCSC Ensembl
Innerchr17:30708220..30792312hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3884093
hg1984093
hg1884093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3142n100
Supporting Variantsnssv3561109, nssv3561112, nssv3561110, nssv3561111, nssv3561107, nssv3561108, nssv3720057, nssv3561113, nssv3720056
Samples
Known GenesSLFN11, SLFN12, SLFN13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055525
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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