A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552264



Internal ID16339673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122585191..122598393hg38UCSC Ensembl
Innerchr10:124344707..124357909hg19UCSC Ensembl
Innerchr10:124334697..124347899hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3813203
hg1913203
hg1813203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1410n54
Supporting Variantsnssv760452, nssv760451
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552264
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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