A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953711



Internal ID16955898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155560540..155573939hg38UCSC Ensembl
OuterchrX:154790201..154803600hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000324
SamplesBILGI_BIOE
Known GenesTMLHE
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953711
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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