A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015745



Internal ID19104963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179076161..179092186hg38UCSC Ensembl
Innerchr5:178503162..178519187hg19UCSC Ensembl
Innerchr5:178435768..178451793hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3816026
hg1916026
hg1816026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5846n100
Supporting Variantsnssv3649300
Samples
Known GenesZNF354C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015745
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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