A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050837



Internal ID18793368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124678954..124828763hg38UCSC Ensembl
Innerchr10:126367523..126517332hg19UCSC Ensembl
Innerchr10:126357513..126507322hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38149810
hg19149810
hg18149810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517373
Samples
Known GenesFAM175B, FAM53B, METTL10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050837
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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