A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624721



Internal ID15848257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:32264334..32267281hg38UCSC Ensembl
Outerchr10:32553262..32556209hg19UCSC Ensembl
Outerchr10:32593268..32596215hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg382948
hg192948
hg182948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512158
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624721
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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