A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv755877



Internal ID15703147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93785779..93792896hg38UCSC Ensembl
Innerchr10:95545536..95552653hg19UCSC Ensembl
Innerchr10:95535526..95542643hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg387118
hg197118
hg187118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551945
Supporting Variants
Samples
Known GenesLGI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv755877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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