A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566109



Internal ID18864390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54851893..54894886hg38UCSC Ensembl
Innerchr17:52929254..52972247hg19UCSC Ensembl
Innerchr17:50284253..50327246hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3842994
hg1942994
hg1842994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060394
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566109
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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