A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022260



Internal ID19111478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25933573..25998816hg38UCSC Ensembl
Innerchr5:25933682..25998925hg19UCSC Ensembl
Innerchr5:25969439..26034682hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3865244
hg1965244
hg1865244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635959, nssv3635958
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)nsv1022260
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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