A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113034



Internal ID18923984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:3902159..3927059hg38UCSC Ensembl
OuterchrX:3820200..3845100hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3824901
hg1924901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967924
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113034
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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