A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141702



Internal ID19267905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:116941232..116946932hg38UCSC Ensembl
OuterchrX:116075200..116080900hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4282n106
Supporting Variantsnssv3993208
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141702
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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