A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056952



Internal ID19146171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357088..35439187hg38UCSC Ensembl
Innerchr17:33684107..33766206hg19UCSC Ensembl
Innerchr17:30708220..30790319hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3882100
hg1982100
hg1882100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3142n100
Supporting Variantsnssv3561106, nssv3561103, nssv3561104, nssv3561105, nssv3561101, nssv3720055, nssv3561102
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)nsv1056952
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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