A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760452



Internal ID16054408
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 StatusS
Merged Variantsnsv552264
Supporting Variants
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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