A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124525



Internal ID18919595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150860264..150860318hg38UCSC Ensembl
OuterchrX:150028737..150028791hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976578
SamplesKWS2
Known GenesCD99L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124525
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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