A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760433



Internal ID16054389
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 StatusS
Merged Variantsnsv552257
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)nssv760433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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