A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552257



Internal ID16339666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122584746..122591655hg38UCSC Ensembl
Innerchr10:124344262..124351171hg19UCSC Ensembl
Innerchr10:124334252..124341161hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386910
hg196910
hg186910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1411n54
Supporting Variantsnssv760432, nssv760433
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552257
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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