A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568608



Internal ID18866889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51028732..51086311hg38UCSC Ensembl
Innerchr17:49106093..49163672hg19UCSC Ensembl
Innerchr17:46461092..46518671hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3857580
hg1957580
hg1857580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055743
Supporting Variants
Samples
Known GenesSPAG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568608
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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