A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551532



Internal ID15992255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74477740..74614146hg38UCSC Ensembl
Innerchr10:76237498..76373904hg19UCSC Ensembl
Innerchr10:75907504..76043910hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38136407
hg19136407
hg18136407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1266n54
Supporting Variantsnssv750292
Samples
Known GenesADK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551532
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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