A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137702



Internal ID18910303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155571739..155573339hg38UCSC Ensembl
OuterchrX:154801400..154803000hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990202
SamplesKWS2
Known GenesTMLHE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137702
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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