A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561075



Internal ID18859356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357088..35430104hg38UCSC Ensembl
Innerchr17:33684107..33757123hg19UCSC Ensembl
Innerchr17:30708220..30781236hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3873017
hg1973017
hg1873017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062593
Supporting Variants
Samples
Known GenesSLFN11, SLFN12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561075
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer