A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141108



Internal ID19284935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10181136..10181263hg38UCSC Ensembl
OuterchrY:10018745..10018872hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992616
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141108
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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