A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551840



Internal ID15992563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88718726..88841108hg38UCSC Ensembl
Innerchr10:90478483..90600865hg19UCSC Ensembl
Innerchr10:90468463..90590845hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38122383
hg19122383
hg18122383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753223
Samples
Known GenesANKRD22, LIPK, LIPM, LIPN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551840
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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