A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953691



Internal ID17302565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:115883968..115889167hg38UCSC Ensembl
OuterchrX:115000301..115005500hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999497
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953691
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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