A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749378



Internal ID16043334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65415683..65440011hg38UCSC Ensembl
Innerchr10:67175441..67199769hg19UCSC Ensembl
Innerchr10:66845447..66869775hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3824329
hg1924329
hg1824329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551250
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)nssv749378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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