A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760436



Internal ID16054392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122584746..122592081hg38UCSC Ensembl
Innerchr10:124344262..124351597hg19UCSC Ensembl
Innerchr10:124334252..124341587hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg387336
hg197336
hg187336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552258
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)nssv760436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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