A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110114



Internal ID19257867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11379944..11380051hg38UCSC Ensembl
OuterchrY:13535620..13535727hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4349n106
Supporting Variantsnssv3959379
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110114
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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