A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953394



Internal ID17302268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:1637208..1640407hg38UCSC Ensembl
OuterchrX:1756101..1759300hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000867
SamplesBILGI_BIOE
Known GenesASMT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953394
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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