A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748615



Internal ID16042571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57094024..57159139hg38UCSC Ensembl
Innerchr10:58853784..58918899hg19UCSC Ensembl
Innerchr10:58523790..58588905hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3865116
hg1965116
hg1865116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551107
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)nssv748615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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