A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560431



Internal ID18858712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17405670..17445234hg38UCSC Ensembl
Innerchr17:17308984..17348548hg19UCSC Ensembl
Innerchr17:17249709..17289273hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3839565
hg1939565
hg1839565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058804
Supporting Variants
Samples
Known GenesSMCR9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560431
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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