A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760309



Internal ID16054265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121677939..121701552hg38UCSC Ensembl
Innerchr10:123437453..123461066hg19UCSC Ensembl
Innerchr10:123427443..123451056hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3823614
hg1923614
hg1823614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552242
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)nssv760309
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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