A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129103



Internal ID19277011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151330328..151335028hg38UCSC Ensembl
OuterchrX:150498800..150503500hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384701
hg194701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4321n106
Supporting Variantsnssv3961777
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129103
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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