A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141116



Internal ID19252469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:17337162..17337228hg38UCSC Ensembl
OuterchrY:19449042..19449108hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992623
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141116
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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