A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760429



Internal ID15707699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122522412..122617922hg38UCSC Ensembl
Innerchr10:124281928..124377438hg19UCSC Ensembl
Innerchr10:124271918..124367428hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3895511
hg1995511
hg1895511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552255
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)nssv760429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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