A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956169



Internal ID17305042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11148415..11167770hg38UCSC Ensembl
OuterchrY:13304091..13323446hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3819356
hg1919356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002514
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956169
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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