A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv755970



Internal ID16049926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95110808..95160441hg38UCSC Ensembl
Innerchr10:96870565..96920198hg19UCSC Ensembl
Innerchr10:96860555..96910188hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3849634
hg1949634
hg1849634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551985
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv755970
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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