A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133762



Internal ID19273477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:29420783..29423583hg38UCSC Ensembl
OuterchrX:29438900..29441700hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969336
SamplesKWS2
Known GenesIL1RAPL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133762
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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