A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953097



Internal ID17301971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:18990615..18993114hg38UCSC Ensembl
OuterchrY:21152501..21155000hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000385
SamplesBILGI_BIOE
Known GenesCD24, TTTY14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953097
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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