A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054984



Internal ID19144203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88362755..88518281hg38UCSC Ensembl
Innerchr10:90122512..90278038hg19UCSC Ensembl
Innerchr10:90112492..90268018hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38155527
hg19155527
hg18155527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706187
Samples
Known GenesRNLS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054984
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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