A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745852



Internal ID19044133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25175037..25226025hg38UCSC Ensembl
Innerchr5:25175146..25226134hg19UCSC Ensembl
Innerchr5:25210903..25261891hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3850989
hg1950989
hg1850989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017026
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)nssv3745852
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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