A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526950



Internal ID15454243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161509955..161525250hg38UCSC Ensembl
Innerchr1:161479745..161495040hg19UCSC Ensembl
Innerchr1:159746369..159761664hg18UCSC Ensembl
Innerchr1:158292800..158308095hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3815296
hg1915296
hg1815296
hg1715296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv17n21
Supporting Variantsnssv703321
Samples
Known GenesFCGR2A, HSPA6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526950
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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