A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055467



Internal ID19144686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65635192..65664112hg38UCSC Ensembl
Innerchr17:63631310..63660230hg19UCSC Ensembl
Innerchr17:61061772..61090692hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3828921
hg1928921
hg1828921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567730
Samples
Known GenesCEP112
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055467
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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