A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626877



Internal ID15850410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:145990477..145990954hg38UCSC Ensembl
OuterchrX:145071995..145072472hg19UCSC Ensembl
OuterchrX:144879687..144880164hg18UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38975
hg19975
hg18975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513625
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)nssv626877
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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