A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054588



Internal ID19143807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56569449..56722996hg38UCSC Ensembl
Innerchr10:58329209..58482756hg19UCSC Ensembl
Innerchr10:57999215..58152762hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38153548
hg19153548
hg18153548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869n100
Supporting Variantsnssv3518335, nssv3504433, nssv3520961
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)nsv1054588
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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