A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513624



Internal ID15853046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:137315083..137316348hg38UCSC Ensembl
OuterchrX:136397242..136398507hg19UCSC Ensembl
OuterchrX:136224908..136226173hg18UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg381465
hg191465
hg181465
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626876
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)nsv513624
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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