A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552272



Internal ID16339681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122587687..122597291hg38UCSC Ensembl
Innerchr10:124347203..124356807hg19UCSC Ensembl
Innerchr10:124337193..124346797hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg389605
hg199605
hg189605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1412n54
Supporting Variantsnssv760471
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552272
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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