A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957824



Internal ID17306697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9791952..9792080hg38UCSC Ensembl
OuterchrX:9759992..9760120hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002490
SamplesBILGI_BIOE
Known GenesSHROOM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957824
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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