A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560052



Internal ID18511647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:780240..832122hg38UCSC Ensembl
Innerchr17:683480..735362hg19UCSC Ensembl
Innerchr17:630230..682112hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3851883
hg1951883
hg1851883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058033
Supporting Variants
Samples
Known GenesGLOD4, NXN, RNMTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560052
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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