A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521283



Internal ID15101890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43371080..43376550hg38UCSC Ensembl
Innerchr10:43866528..43871998hg19UCSC Ensembl
Innerchr10:43186534..43192004hg18UCSC Ensembl
Innerchr10:43186534..43192004hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385471
hg195471
hg185471
hg175471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697885
Samples
Known GenesFXYD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521283
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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