A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140097



Internal ID19261731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11272124..11331224hg38UCSC Ensembl
OuterchrY:13427800..13486900hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3859101
hg1959101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978808
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140097
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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