A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141052



Internal ID18926089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:17484630..17484699hg38UCSC Ensembl
OuterchrX:17502753..17502822hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992566, nssv3986988
SamplesKWS1, KWS2
Known GenesNHS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141052
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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