A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512671



Internal ID15852096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:16409134..16410364hg38UCSC Ensembl
OuterchrX:16427257..16428487hg19UCSC Ensembl
OuterchrX:16337178..16338408hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381231
hg191231
hg181231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625291
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)nsv512671
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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