A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624712



Internal ID15501562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14199066..14200992hg38UCSC Ensembl
Outerchr10:14241065..14242991hg19UCSC Ensembl
Outerchr10:14281071..14282997hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381927
hg191927
hg181927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512149
Supporting Variants
Samples1
Known GenesFRMD4A
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624712
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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