A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957791



Internal ID17306664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:58534660..58534761hg38UCSC Ensembl
OuterchrX:58561093..58561194hg19UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002457
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957791
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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