A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953088



Internal ID17301962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11396525..11402124hg38UCSC Ensembl
OuterchrY:13552201..13557800hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000376
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953088
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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