A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115266



Internal ID18902799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:54082965..54083035hg38UCSC Ensembl
OuterchrX:54109398..54109468hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976316
SamplesKWS2
Known GenesFAM120C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115266
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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