A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017026



Internal ID19106243
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 StatusM
Merged Variants
Supporting Variantsnssv3745852, nssv3745853, nssv3635955
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)nsv1017026
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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