A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956173



Internal ID17305046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11305667..11327534hg38UCSC Ensembl
OuterchrY:13461343..13483210hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3821868
hg1921868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002517
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956173
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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