A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551480



Internal ID16338889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70555458..70584823hg38UCSC Ensembl
Innerchr10:72315214..72344579hg19UCSC Ensembl
Innerchr10:71985220..72014585hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3829366
hg1929366
hg1829366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174247
SamplesNINDS_173
Known GenesPALD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551480
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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