A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067378



Internal ID19156597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14105271..14152192hg38UCSC Ensembl
Innerchr17:14008588..14055509hg19UCSC Ensembl
Innerchr17:13949313..13996234hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3846922
hg1946922
hg1846922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560361
Samples
Known GenesCOX10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067378
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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