A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560079



Internal ID18511674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2359823..2390866hg38UCSC Ensembl
Innerchr17:2263117..2294160hg19UCSC Ensembl
Innerchr17:2209867..2240910hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3831044
hg1931044
hg1831044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066475
Supporting Variants
Samples
Known GenesMNT, SGSM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560079
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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