A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957346



Internal ID17306219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10628552..10628650hg38UCSC Ensembl
OuterchrY:13139066..13139164hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002567
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957346
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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