A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118400



Internal ID19266906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:114043008..114043057hg38UCSC Ensembl
OuterchrX:113286182..113286234hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3850
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958894
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118400
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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