A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115288



Internal ID19274768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:123181907..123181958hg38UCSC Ensembl
OuterchrX:122315760..122315811hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976338, nssv3987013
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115288
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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