A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750272



Internal ID16044228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72627440..72638174hg38UCSC Ensembl
Innerchr10:74387198..74397932hg19UCSC Ensembl
Innerchr10:74057204..74067938hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3810735
hg1910735
hg1810735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551515
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)nssv750272
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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