A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141662



Internal ID19284079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:11707380..11713080hg38UCSC Ensembl
OuterchrX:11725500..11731200hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4210n106
Supporting Variantsnssv3993167
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141662
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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