A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128558



Internal ID18909137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155560499..155560768hg38UCSC Ensembl
OuterchrX:154790160..154790429hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960464
SamplesKWS1
Known GenesTMLHE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128558
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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