A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551533



Internal ID15992256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74487347..74612279hg38UCSC Ensembl
Innerchr10:76247105..76372037hg19UCSC Ensembl
Innerchr10:75917111..76042043hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38124933
hg19124933
hg18124933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1266n54
Supporting Variantsnssv1174255
SamplesNINDS_145
Known GenesADK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551533
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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